A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620669



Internal ID7007539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73402717..73412725hg38UCSC Ensembl
Innerchr9:73402719..73412724hg38UCSC Ensembl
Outerchr9:73402716..73412727hg38UCSC Ensembl
chr9:76017633..76027641hg19UCSC Ensembl
Innerchr9:76017635..76027640hg19UCSC Ensembl
Outerchr9:76017632..76027643hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3810009
hg1910009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13518772, essv13518759, essv13518767, essv13518777, essv13518771, essv13518770, essv13518785, essv13518751, essv13518774, essv13518748, essv13518791, essv13518762, essv13518784, essv13518786, essv13518781, essv13518788, essv13518765, essv13518789, essv13518749, essv13518769, essv13518761, essv13518790, essv13518753, essv13518779, essv13518780, essv13518773, essv13518783, essv13518787, essv13518763, essv13518782, essv13518760, essv13518764, essv13518768, essv13518756, essv13518766, essv13518775, essv13518778, essv13518755, essv13518757, essv13518750, essv13518776, essv13518758, essv13518752, essv13518754
SamplesNA20588, NA12717, HG01521, HG01918, HG00231, NA11933, HG02231, HG01389, NA20813, NA20512, NA12751, HG01486, HG02734, NA12400, HG00327, HG01702, NA20812, HG01133, HG01626, HG00326, HG00178, HG01524, HG01353, NA12489, HG01612, NA12718, NA12829, NA12249, HG01101, HG01705, HG01680, HG01403, NA19625, HG00336, HG00742, HG00366, HG01357, NA20778, HG00319, NA20803, HG00378, HG01085, HG01631, HG01479
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620669
Frequency
Sample Size2504
Observed Gain0
Observed Loss44
Observed Complex0
Frequencyn/a


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