A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661696



Internal ID9927801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41084781..41084971hg38UCSC Ensembl
chr5:41084883..41085073hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5764361, essv5867736, essv6357925, essv5525776, essv5753413, essv6144086, essv5700652, essv6442826, essv6443662, essv6109429, essv5474210, essv6111567, essv5989226, essv5973515, essv5504137, essv6215317, essv5687861, essv5635529, essv6012109, essv5827687, essv5707838, essv5483483, essv5503574, essv6241997, essv6318553, essv6339107, essv5624136, essv6178950, essv6521619, essv5846557, essv6294395, essv5534712, essv5495499
SamplesNA18502, NA19399, NA18486, NA19393, NA20332, NA19190, NA19374, NA19373, NA19379, NA18916, NA19197, NA20291, NA19189, NA20342, HG01124, NA19210, NA19403, NA19257, NA20296, NA19401, NA19390, NA18909, NA19435, NA19334, NA19311, NA19376, NA19328, NA19468, NA19116, NA19430, NA18505, NA19129, NA18488
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661696
Frequency
Sample Size1151
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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