A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590640



Internal ID16031363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:74105982..74172342hg38UCSC Ensembl
Innerchr3:74155133..74221493hg19UCSC Ensembl
Innerchr3:74237823..74304183hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3866361
hg1966361
hg1866361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965599
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590640
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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