A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526859



Internal ID15454152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:118550083..118558182hg38UCSC Ensembl
Innerchr2:119307659..119315758hg19UCSC Ensembl
Innerchr2:119024129..119032228hg18UCSC Ensembl
Innerchr2:119023889..119031988hg17UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg388100
hg198100
hg188100
hg178100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703217
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526859
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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