A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591596



Internal ID16032319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128153332..128163221hg38UCSC Ensembl
Innerchr3:127872175..127882064hg19UCSC Ensembl
Innerchr3:129354865..129364754hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg389890
hg199890
hg189890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv972960
Samples
Known GenesEEFSEC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591596
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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