A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700709



Internal ID15437361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34324694..34389027hg38UCSC Ensembl
Innerchr1:34790295..34854628hg19UCSC Ensembl
Innerchr1:34562882..34627215hg18UCSC Ensembl
Innerchr1:34459388..34523721hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3864334
hg1964334
hg1864334
hg1764334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524723
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700709
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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