A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848203



Internal ID15795473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90166313..90210523hg38UCSC Ensembl
Innerchr15:90709545..90753755hg19UCSC Ensembl
Innerchr15:88510549..88554759hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3844211
hg1944211
hg1844211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570390
Supporting Variants
Samples
Known GenesSEMA4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv848203
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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