A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527078



Internal ID15454371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:138643469..138651750hg38UCSC Ensembl
Innerchr5:137979158..137987439hg19UCSC Ensembl
Innerchr5:138007057..138015338hg18UCSC Ensembl
Innerchr5:138007057..138015338hg17UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg388282
hg198282
hg188282
hg178282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703457
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527078
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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