A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703961



Internal ID15440613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:31919232..31929054hg38UCSC Ensembl
Innerchr4:31920854..31930676hg19UCSC Ensembl
Innerchr4:31564752..31574574hg18UCSC Ensembl
Innerchr4:31710923..31720745hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg389823
hg199823
hg189823
hg179823
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527508
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703961
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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