A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520015



Internal ID15447308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22348728..22356537hg38UCSC Ensembl
Innerchr1:22675221..22683030hg19UCSC Ensembl
Innerchr1:22547808..22555617hg18UCSC Ensembl
Innerchr1:22420527..22428336hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg387810
hg197810
hg187810
hg177810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697178
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520015
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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