A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568299



Internal ID16355708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23322889..23427478hg38UCSC Ensembl
Innerchr15:23568030..23672625hg19UCSC Ensembl
Innerchr15:21119471..21224066hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38104590
hg19104596
hg18104596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4331n54
Supporting Variantsnssv838445
Samples
Known GenesGOLGA8S, LOC440243
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568299
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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