A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528961



Internal ID15456254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5494626..5496367hg38UCSC Ensembl
Innerchr5:5494739..5496480hg19UCSC Ensembl
Innerchr5:5547739..5549480hg18UCSC Ensembl
Innerchr5:5547739..5549480hg17UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg381742
hg191742
hg181742
hg171742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705657
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528961
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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