A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv965757



Internal ID16259713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75403949..75587298hg38UCSC Ensembl
Innerchr3:75453100..75636449hg19UCSC Ensembl
Innerchr3:75535790..75719139hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38183350
hg19183350
hg18183350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590690
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)nssv965757
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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