A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705709



Internal ID15442361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:95315661..95339446hg38UCSC Ensembl
Innerchr1:95781217..95805002hg19UCSC Ensembl
Innerchr1:95553805..95577590hg18UCSC Ensembl
Innerchr1:95493238..95517023hg17UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3823786
hg1923786
hg1823786
hg1723786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv529002
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705709
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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