A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523255



Internal ID15450548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:159453103..159467352hg38UCSC Ensembl
Innerchr4:160374255..160388504hg19UCSC Ensembl
Innerchr4:160593705..160607954hg18UCSC Ensembl
Innerchr4:160731860..160746109hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3814250
hg1914250
hg1814250
hg1714250
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698984
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523255
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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