A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522588



Internal ID15449881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144113734..144114933hg38UCSC Ensembl
Innerchr6:144434871..144436070hg19UCSC Ensembl
Innerchr6:144476564..144477763hg18UCSC Ensembl
Innerchr6:144476564..144477763hg17UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg381200
hg191200
hg181200
hg171200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705975
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522588
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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