A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv850997



Internal ID15798267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100879313..100880220hg38UCSC Ensembl
Innerchr15:101419518..101420425hg19UCSC Ensembl
Innerchr15:99237041..99237948hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38908
hg19908
hg18908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570814
Supporting Variants
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv850997
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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