A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659107



Internal ID9925212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:80367251..80371707hg38UCSC Ensembl
Outerchr9:80366880..80372077hg38UCSC Ensembl
Innerchr9:82982166..82986622hg19UCSC Ensembl
Outerchr9:82981795..82986992hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg385198
hg195198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5420705, essv5902996, essv6346305, essv6348882, essv6322209, essv5913392, essv6436330, essv6574908, essv5761412, essv5824896, essv6368343, essv6211672, essv5408022, essv5884565, essv6488500, essv6436160, essv5692466, essv5554781, essv5550935, essv6038652, essv6149965, essv5541580, essv6383685, essv6552556, essv5664133
SamplesNA19359, NA19443, NA19315, NA19448, NA19384, NA19371, NA19456, NA19445, NA19462, NA19327, NA19449, NA19453, NA19436, NA19401, NA19440, NA19390, NA19435, NA19331, NA19334, NA19470, NA19428, NA19467, NA19360, NA19438, NA19468
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659107
Frequency
Sample Size1151
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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