A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681777



Internal ID15418429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6346730..6346966hg38UCSC Ensembl
Innerchr10:6388692..6388928hg19UCSC Ensembl
Innerchr10:6428698..6428934hg18UCSC Ensembl
Innerchr10:6428698..6428934hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38237
hg19237
hg18237
hg17237
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519424
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681777
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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