A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676525



Internal ID9942630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62601915..62607021hg38UCSC Ensembl
Outerchr9:62601544..62607391hg38UCSC Ensembl
Innerchr9:46913216..46918322hg19UCSC Ensembl
Outerchr9:46912845..46918692hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385848
hg195848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1349e199
Supporting Variantsessv5890683, essv5605113, essv6198956, essv6560666, essv5572283, essv6562142, essv6206941, essv5536660, essv5991663, essv5669503, essv5998277, essv5419993, essv5876710, essv6017445, essv6244314, essv6108280, essv6596358, essv5711343, essv5612272, essv6093929, essv6370707, essv6300683, essv6549867, essv6315430, essv5812426, essv5411834, essv6351012, essv6572453
SamplesHG01441, HG01359, HG01465, HG01488, HG01354, HG01365, HG01495, HG01550, HG01124, HG01353, HG01136, HG01360, HG01384, HG01498, HG01149, HG01383, HG01497, HG01148, HG01551, HG01375, HG01494, HG01113, HG01137, HG01489, HG01342, HG01254, HG01112, HG01437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676525
Frequency
Sample Size1151
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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