A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839830



Internal ID15787100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34412954..34414928hg38UCSC Ensembl
Innerchr15:34705155..34707129hg19UCSC Ensembl
Innerchr15:32492447..32494421hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381975
hg191975
hg181975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568949
Supporting Variants
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839830
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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