A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698707



Internal ID15435359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:4353653..4358654hg38UCSC Ensembl
Innerchr4:4355380..4360381hg19UCSC Ensembl
Innerchr4:4406281..4411282hg18UCSC Ensembl
Innerchr4:4473452..4478453hg17UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg385002
hg195002
hg185002
hg175002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523027
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698707
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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