A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839796



Internal ID15787066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32952471..33154770hg38UCSC Ensembl
Innerchr15:33244672..33446971hg19UCSC Ensembl
Innerchr15:31031964..31234263hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38202300
hg19202300
hg18202300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568918
Supporting Variants
Samples
Known GenesFMN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839796
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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