A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695494



Internal ID15085460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114816430..114822743hg38UCSC Ensembl
Innerchr10:116576189..116582502hg19UCSC Ensembl
Innerchr10:116566179..116572492hg18UCSC Ensembl
Innerchr10:116566179..116572492hg17UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg386314
hg196314
hg186314
hg176314
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518081
Supporting Variants
Samples
Known GenesFAM160B1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695494
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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