A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527582



Internal ID15454875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:157610404..157612729hg38UCSC Ensembl
Innerchr5:157037412..157039737hg19UCSC Ensembl
Innerchr5:156969990..156972315hg18UCSC Ensembl
Innerchr5:156969990..156972315hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382326
hg192326
hg182326
hg172326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704043
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527582
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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