A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634894



Internal ID7021694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72866240..72867102hg38UCSC Ensembl
Innerchr14:72866241..72867102hg38UCSC Ensembl
Outerchr14:72866240..72867103hg38UCSC Ensembl
chr14:73332948..73333810hg19UCSC Ensembl
Innerchr14:73332949..73333810hg19UCSC Ensembl
Outerchr14:73332948..73333811hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15055604, essv15055514, essv15055543, essv15055540, essv15055524, essv15055566, essv15055557, essv15055506, essv15055609, essv15055592, essv15055579, essv15055499, essv15055504, essv15055516, essv15055575, essv15055565, essv15055559, essv15055503, essv15055523, essv15055525, essv15055571, essv15055582, essv15055520, essv15055577, essv15055608, essv15055537, essv15055532, essv15055585, essv15055551, essv15055549, essv15055513, essv15055573, essv15055593, essv15055517, essv15055507, essv15055552, essv15055600, essv15055590, essv15055501, essv15055576, essv15055534, essv15055578, essv15055505, essv15055518, essv15055601, essv15055542, essv15055531, essv15055572, essv15055605, essv15055538, essv15055596, essv15055502, essv15055580, essv15055564, essv15055519, essv15055611, essv15055547, essv15055530, essv15055612, essv15055554, essv15055546, essv15055536, essv15055515, essv15055500, essv15055556, essv15055598, essv15055563, essv15055581, essv15055535, essv15055594, essv15055508, essv15055597, essv15055545, essv15055583, essv15055539, essv15055561, essv15055528, essv15055570, essv15055550, essv15055610, essv15055588, essv15055606, essv15055529, essv15055607, essv15055595, essv15055553, essv15055589, essv15055599, essv15055544, essv15055521, essv15055574, essv15055527, essv15055591, essv15055567, essv15055584, essv15055560, essv15055613, essv15055541, essv15055522, essv15055568, essv15055558, essv15055555, essv15055526, essv15055512, essv15055603, essv15055548, essv15055586, essv15055562, essv15055602, essv15055533, essv15055587, essv15055510, essv15055511, essv15055509, essv15055569
SamplesHG01747, HG01608, HG03690, HG00304, HG00121, HG00102, HG01773, NA12414, HG01602, HG01586, NA20531, HG02012, NA12340, NA20808, HG02734, NA12400, NA12413, NA12813, HG00127, HG00356, HG00251, HG00122, NA19315, NA20589, NA20774, HG01168, NA20769, NA12348, NA20768, NA19771, HG01528, HG04131, HG00243, NA20518, NA06984, NA19917, HG01525, HG01259, NA20889, HG00118, NA20757, HG00323, NA18867, HG01164, HG00260, HG00313, HG00133, NA12777, HG01136, HG00290, NA20535, NA19657, HG01867, HG00268, HG02233, HG01247, NA12342, NA20505, NA19175, HG02236, NA12872, HG00190, NA19984, NA18644, HG01879, HG01612, HG01989, NA12718, HG01102, HG03829, HG00273, NA11919, HG00250, NA20581, NA12829, HG01504, HG02657, HG01130, HG01705, NA19761, NA06985, NA19318, HG00099, NA12778, HG00246, HG01075, HG01858, HG00382, NA20801, NA12716, HG00254, HG00285, HG04006, HG01980, HG02223, HG00742, HG02220, HG00136, HG00278, HG03846, NA20803, NA12874, NA07037, HG04003, HG00125, HG00107, NA19785, HG01556, HG02107, HG02182, HG02052, HG00274, NA18488, HG02351, HG01672
Known GenesDPF3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634894
Frequency
Sample Size2504
Observed Gain0
Observed Loss115
Observed Complex0
Frequencyn/a


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