A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526972



Internal ID15454265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38783041..38785292hg38UCSC Ensembl
Innerchr1:39248713..39250964hg19UCSC Ensembl
Innerchr1:39021300..39023551hg18UCSC Ensembl
Innerchr1:38917806..38920057hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382252
hg192252
hg182252
hg172252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703344
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526972
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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