A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152029



Internal ID15879079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162415287..162508329hg38UCSC Ensembl
Innerchr3:162133075..162226117hg19UCSC Ensembl
Innerchr3:163615769..163708811hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3893043
hg1993043
hg1893043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592189
Supporting Variants
SamplesHGDP01304
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152029
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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