A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149238



Internal ID15878091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70241093..70305902hg38UCSC Ensembl
Innerchr15:70533432..70598241hg19UCSC Ensembl
Innerchr15:68320486..68385295hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3864810
hg1964810
hg1864810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569814
Supporting Variants
SamplesHGDP01094
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149238
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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