A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515827



Internal ID15442884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:201243708..201248020hg38UCSC Ensembl
Innerchr1:201212836..201217148hg19UCSC Ensembl
Innerchr1:199479459..199483771hg18UCSC Ensembl
Innerchr1:197944493..197948805hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg384313
hg194313
hg184313
hg174313
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662306, nssv692309, nssv675865, nssv654896, nssv673889, nssv664909
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515827
Frequency
Sample Size2026
Observed Gain2
Observed Loss4
Observed Complex0
Frequencyn/a


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