A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523600



Internal ID15450893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104197383..104238145hg38UCSC Ensembl
Innerchr1:104740005..104780767hg19UCSC Ensembl
Innerchr1:104541528..104582290hg18UCSC Ensembl
Innerchr1:104452026..104492788hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3840763
hg1940763
hg1840763
hg1740763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699393
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523600
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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