A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522136



Internal ID15449429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180362741..180415292hg38UCSC Ensembl
Innerchr4:181283894..181336445hg19UCSC Ensembl
Innerchr4:181520888..181573439hg18UCSC Ensembl
Innerchr4:181659043..181711594hg17UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3852552
hg1952552
hg1852552
hg1752552
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694910
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522136
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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