A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526481



Internal ID15453774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71095473..71120755hg38UCSC Ensembl
Innerchr10:72855230..72880512hg19UCSC Ensembl
Innerchr10:72525236..72550518hg18UCSC Ensembl
Innerchr10:72525236..72550518hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3825283
hg1925283
hg1825283
hg1725283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702790
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526481
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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