A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656508



Internal ID15393160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46332377hg38UCSC Ensembl
Innerchr10:47543322..47703613hg19UCSC Ensembl
Innerchr10:47013328..47173619hg18UCSC Ensembl
Innerchr10:47013328..47173619hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38160292
hg19160292
hg18160292
hg17160292
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516485
Supporting Variants
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656508
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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