A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516575



Internal ID15443868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22262500..22271564hg38UCSC Ensembl
Innerchr1:22588993..22598057hg19UCSC Ensembl
Innerchr1:22461580..22470644hg18UCSC Ensembl
Innerchr1:22334299..22343363hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg389065
hg199065
hg189065
hg179065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669268, nssv674738
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516575
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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