A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520237



Internal ID15447530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:78173560..78194439hg38UCSC Ensembl
Innerchr1:78639244..78660123hg19UCSC Ensembl
Innerchr1:78411832..78432711hg18UCSC Ensembl
Innerchr1:78351265..78372144hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3820880
hg1920880
hg1820880
hg1720880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673864, nssv662070
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520237
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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