A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv981182



Internal ID15928452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165740052..165840684hg38UCSC Ensembl
Innerchr3:165457840..165558472hg19UCSC Ensembl
Innerchr3:166940534..167041166hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38100633
hg19100633
hg18100633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592481
Supporting Variants
Samples
Known GenesBCHE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv981182
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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