A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653687



Internal ID15390339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25555425..25576891hg38UCSC Ensembl
Innerchr4:25557047..25578513hg19UCSC Ensembl
Innerchr4:25166145..25187611hg18UCSC Ensembl
Innerchr4:25233316..25254782hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3821467
hg1921467
hg1821467
hg1721467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517048
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653687
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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