A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591856



Internal ID16379265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:139282002..139318990hg38UCSC Ensembl
Innerchr3:139000844..139037832hg19UCSC Ensembl
Innerchr3:140483534..140520522hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3836989
hg1936989
hg1836989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv974772
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591856
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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