A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591374



Internal ID16378783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119632803..119635586hg38UCSC Ensembl
Innerchr3:119351650..119354433hg19UCSC Ensembl
Innerchr3:120834340..120837123hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg382784
hg192784
hg182784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8519n54
Supporting Variantsnssv971725
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591374
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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