A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv965677



Internal ID16259633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75397370..75566147hg38UCSC Ensembl
Innerchr3:75446521..75615298hg19UCSC Ensembl
Innerchr3:75529211..75697988hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38168778
hg19168778
hg18168778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590666
Supporting Variants
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv965677
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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