A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591857



Internal ID16379266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:139692189..139736484hg38UCSC Ensembl
Innerchr3:139411031..139455326hg19UCSC Ensembl
Innerchr3:140893721..140938016hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3844296
hg1944296
hg1844296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152542
Samples1780862202_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591857
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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