A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591853



Internal ID16032576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138381697..138475593hg38UCSC Ensembl
Innerchr3:138100539..138194435hg19UCSC Ensembl
Innerchr3:139583229..139677125hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3893897
hg1993897
hg1893897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv974769
Samples
Known GenesESYT3, MRAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591853
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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