A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696908



Internal ID15433560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104449028..104467015hg38UCSC Ensembl
Innerchr1:104991650..105009637hg19UCSC Ensembl
Innerchr1:104793173..104811160hg18UCSC Ensembl
Innerchr1:104703671..104721658hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3817988
hg1917988
hg1817988
hg1717988
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519539
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696908
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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