A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv842539



Internal ID15789809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49248019..49257746hg38UCSC Ensembl
Innerchr15:49540216..49549943hg19UCSC Ensembl
Innerchr15:47327508..47337235hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg389728
hg199728
hg189728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569354
Supporting Variants
Samples
Known GenesGALK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv842539
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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