A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527012



Internal ID15454305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:145301995..145323233hg38UCSC Ensembl
Innerchr5:144681558..144702796hg19UCSC Ensembl
Innerchr5:144661751..144682989hg18UCSC Ensembl
Innerchr5:144661751..144682989hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3821239
hg1921239
hg1821239
hg1721239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703387
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527012
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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