A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957771



Internal ID16251727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188618..192626hg38UCSC Ensembl
Innerchr3:230301..234309hg19UCSC Ensembl
Innerchr3:205301..209309hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg384009
hg194009
hg184009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589271
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957771
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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