A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521071



Internal ID15448364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:106549823..106558146hg38UCSC Ensembl
Innerchr1:107092445..107100768hg19UCSC Ensembl
Innerchr1:106893968..106902291hg18UCSC Ensembl
Innerchr1:106804487..106812810hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg388324
hg198324
hg188324
hg178324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697768
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521071
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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