A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527995



Internal ID15455288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6100413..6109815hg38UCSC Ensembl
Innerchr5:6100526..6109928hg19UCSC Ensembl
Innerchr5:6153526..6162928hg18UCSC Ensembl
Innerchr5:6153526..6162928hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg389403
hg199403
hg189403
hg179403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704520
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527995
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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