A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657828



Internal ID15394480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121181867..121197234hg38UCSC Ensembl
Innerchr10:122941381..122956748hg19UCSC Ensembl
Innerchr10:122931371..122946738hg18UCSC Ensembl
Innerchr10:122931371..122946738hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3815368
hg1915368
hg1815368
hg1715368
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517064
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657828
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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