A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620692



Internal ID6660873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74129821..74131974hg38UCSC Ensembl
Innerchr9:74129838..74131958hg38UCSC Ensembl
Outerchr9:74129805..74131991hg38UCSC Ensembl
chr9:76744737..76746890hg19UCSC Ensembl
Innerchr9:76744754..76746874hg19UCSC Ensembl
Outerchr9:76744721..76746907hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382154
hg192154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13522582, essv13522612, essv13522560, essv13522605, essv13522591, essv13522584, essv13522589, essv13522619, essv13522587, essv13522596, essv13522575, essv13522601, essv13522580, essv13522616, essv13522600, essv13522611, essv13522573, essv13522607, essv13522583, essv13522564, essv13522613, essv13522586, essv13522599, essv13522598, essv13522568, essv13522593, essv13522581, essv13522572, essv13522597, essv13522579, essv13522590, essv13522588, essv13522617, essv13522577, essv13522602, essv13522592, essv13522563, essv13522565, essv13522567, essv13522606, essv13522604, essv13522559, essv13522569, essv13522595, essv13522574, essv13522614, essv13522615, essv13522603, essv13522608, essv13522570, essv13522576, essv13522610, essv13522585, essv13522594, essv13522561, essv13522618, essv13522578, essv13522562, essv13522571, essv13522566, essv13522609
SamplesNA19394, HG03096, HG01485, HG02944, NA19700, HG03052, HG03247, HG03300, HG03298, NA19819, HG03190, HG03100, HG02624, HG03069, NA19374, HG03168, HG03135, NA19197, NA18498, HG03224, NA19130, HG02281, HG03520, HG02703, HG03556, HG01495, NA19238, NA19235, NA19901, NA19189, NA18520, HG02427, NA19239, NA18864, NA19908, HG03160, HG02334, NA19391, HG02976, HG02555, HG03382, HG03202, NA19257, NA18523, HG02568, HG03064, HG02255, NA19834, HG03539, HG02983, NA18865, HG03259, NA19324, HG02839, HG02814, HG02771, NA19143, NA19117, NA19900, HG01914, HG01883
Known GenesMIR6130
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620692
Frequency
Sample Size2504
Observed Gain0
Observed Loss61
Observed Complex0
Frequencyn/a


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