A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621700



Internal ID7008567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123854680..123855396hg38UCSC Ensembl
Innerchr9:123854680..123855396hg38UCSC Ensembl
Outerchr9:123854410..123855659hg38UCSC Ensembl
chr9:126616959..126617675hg19UCSC Ensembl
Innerchr9:126616959..126617675hg19UCSC Ensembl
Outerchr9:126616689..126617938hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618535, essv13618529, essv13618530, essv13618536, essv13618557, essv13618496, essv13618505, essv13618585, essv13618490, essv13618543, essv13618531, essv13618488, essv13618498, essv13618595, essv13618523, essv13618597, essv13618565, essv13618600, essv13618509, essv13618570, essv13618539, essv13618495, essv13618577, essv13618510, essv13618592, essv13618564, essv13618511, essv13618599, essv13618593, essv13618579, essv13618563, essv13618587, essv13618517, essv13618494, essv13618569, essv13618532, essv13618576, essv13618514, essv13618562, essv13618594, essv13618598, essv13618502, essv13618584, essv13618503, essv13618521, essv13618497, essv13618524, essv13618525, essv13618540, essv13618572, essv13618522, essv13618603, essv13618547, essv13618586, essv13618555, essv13618573, essv13618549, essv13618602, essv13618583, essv13618528, essv13618520, essv13618606, essv13618506, essv13618560, essv13618493, essv13618501, essv13618558, essv13618504, essv13618526, essv13618546, essv13618550, essv13618567, essv13618590, essv13618548, essv13618596, essv13618518, essv13618568, essv13618605, essv13618553, essv13618508, essv13618574, essv13618516, essv13618519, essv13618534, essv13618527, essv13618588, essv13618515, essv13618492, essv13618601, essv13618500, essv13618507, essv13618512, essv13618533, essv13618486, essv13618545, essv13618487, essv13618591, essv13618604, essv13618551, essv13618578, essv13618561, essv13618575, essv13618556, essv13618581, essv13618589, essv13618538, essv13618559, essv13618571, essv13618554, essv13618499, essv13618544, essv13618566, essv13618489, essv13618552, essv13618491, essv13618541, essv13618580, essv13618537, essv13618542, essv13618582, essv13618513
SamplesNA19394, HG02339, NA19028, HG03484, HG03121, HG03548, NA18508, HG02702, NA18507, NA18881, HG03300, HG02852, HG02419, HG03558, HG03130, NA20298, NA19819, HG03455, HG03190, NA18878, NA18504, HG03518, HG00737, HG03577, HG01461, NA19098, NA20356, NA19920, HG03074, HG01350, HG01366, NA19201, HG02811, NA19119, HG02595, HG02860, HG03342, NA19457, HG03224, NA19130, NA19038, HG03209, HG03460, HG02703, NA19383, HG03189, HG02315, HG03268, NA19172, HG03352, HG01259, NA19189, HG02427, NA20355, HG03055, NA20318, HG03270, NA19210, NA18934, HG01095, HG03291, HG01882, NA19043, NA19236, HG02554, HG02322, NA18516, HG03159, HG03027, HG02497, HG01889, NA18907, HG03301, NA19114, NA18879, HG03476, HG03202, HG02881, HG02283, NA19320, NA19099, HG03451, HG03391, HG01890, NA18523, NA19095, HG02635, NA19395, HG01956, NA19401, HG02613, NA19309, HG02282, NA19321, NA19108, NA19149, HG02983, HG01894, HG02721, NA19037, HG03259, HG02982, HG03433, HG02941, HG02580, NA19117, HG03565, HG03039, NA19248, HG02970, NA19472, NA19223, NA20334, HG02768, HG03410, HG03162, NA19146, NA19312, HG01125, HG03198, HG02006
Known GenesDENND1A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621700
Frequency
Sample Size2504
Observed Gain0
Observed Loss121
Observed Complex0
Frequencyn/a


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