A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524640



Internal ID15105247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:168721928..168754881hg38UCSC Ensembl
Innerchr4:169643079..169676032hg19UCSC Ensembl
Innerchr4:169879654..169912607hg18UCSC Ensembl
Innerchr4:170017809..170050762hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3832954
hg1932954
hg1832954
hg1732954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700605
Samples
Known GenesPALLD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524640
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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