A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590635



Internal ID16378044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:73202838..73238687hg38UCSC Ensembl
Innerchr3:73251989..73287838hg19UCSC Ensembl
Innerchr3:73334679..73370528hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3835850
hg1935850
hg1835850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965593
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590635
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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