A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686480



Internal ID15423132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:76704332..76724665hg38UCSC Ensembl
Innerchr1:77170017..77190350hg19UCSC Ensembl
Innerchr1:76942605..76962938hg18UCSC Ensembl
Innerchr1:76882038..76902371hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3820334
hg1920334
hg1820334
hg1720334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520575
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686480
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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