A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848198



Internal ID15795468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:88636445..88649425hg38UCSC Ensembl
Innerchr15:89179676..89192656hg19UCSC Ensembl
Innerchr15:86980680..86993660hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3812981
hg1912981
hg1812981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570384
Supporting Variants
Samples
Known GenesISG20
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv848198
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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