A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149616



Internal ID15875740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93812994..93941235hg38UCSC Ensembl
Innerchr15:94356223..94484464hg19UCSC Ensembl
Innerchr15:92157227..92285468hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38128242
hg19128242
hg18128242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570527
Supporting Variants
SamplesHGDP00731
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149616
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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