A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687719



Internal ID15424371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46281263hg38UCSC Ensembl
Innerchr10:47543322..47652499hg19UCSC Ensembl
Innerchr10:47013328..47122505hg18UCSC Ensembl
Innerchr10:47013328..47122505hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38109178
hg19109178
hg18109178
hg17109178
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516485
Supporting Variants
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687719
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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