A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv842441



Internal ID15789711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44109068..44220892hg38UCSC Ensembl
Innerchr15:44401266..44513090hg19UCSC Ensembl
Innerchr15:42188558..42300382hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38111825
hg19111825
hg18111825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569298
Supporting Variants
Samples
Known GenesFRMD5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv842441
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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