A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526491



Internal ID15453784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:178088468..178123550hg38UCSC Ensembl
Innerchr4:179009622..179044704hg19UCSC Ensembl
Innerchr4:179246616..179281698hg18UCSC Ensembl
Innerchr4:179384771..179419853hg17UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3835083
hg1935083
hg1835083
hg1735083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702800
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526491
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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