A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671865



Internal ID15408517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:42051099..42122960hg38UCSC Ensembl
Innerchr1:42516770..42588631hg19UCSC Ensembl
Innerchr1:42289357..42361218hg18UCSC Ensembl
Innerchr1:42185863..42257724hg17UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3871862
hg1971862
hg1871862
hg1771862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519479
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671865
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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