A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591190



Internal ID16378599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:102626794..103227372hg38UCSC Ensembl
Innerchr3:102345638..102946216hg19UCSC Ensembl
Innerchr3:103828328..104428906hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38600579
hg19600579
hg18600579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv970920
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591190
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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