A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592512



Internal ID16379921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172171677..172175233hg38UCSC Ensembl
Innerchr3:171889467..171893023hg19UCSC Ensembl
Innerchr3:173372161..173375717hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg383557
hg193557
hg183557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv981218
Samples
Known GenesFNDC3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592512
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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