A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527784



Internal ID15455077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130309799..130419497hg38UCSC Ensembl
Innerchr4:131230954..131340652hg19UCSC Ensembl
Innerchr4:131450404..131560102hg18UCSC Ensembl
Innerchr4:131588559..131698257hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38109699
hg19109699
hg18109699
hg17109699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704275
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527784
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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