A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696260



Internal ID15432912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:117201532..117282921hg38UCSC Ensembl
Innerchr4:118122688..118204077hg19UCSC Ensembl
Innerchr4:118342136..118423525hg18UCSC Ensembl
Innerchr4:118480291..118561680hg17UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3881390
hg1981390
hg1881390
hg1781390
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518806
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696260
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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