A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521412



Internal ID15448705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3665823..3668434hg38UCSC Ensembl
Innerchr10:3708015..3710626hg19UCSC Ensembl
Innerchr10:3698015..3700626hg18UCSC Ensembl
Innerchr10:3698015..3700626hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg382612
hg192612
hg182612
hg172612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694443
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521412
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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