A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525857



Internal ID15453150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:171567301..171567778hg38UCSC Ensembl
Innerchr2:172423811..172424288hg19UCSC Ensembl
Innerchr2:172132057..172132534hg18UCSC Ensembl
Innerchr2:172249318..172249795hg17UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38478
hg19478
hg18478
hg17478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702052
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525857
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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