A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591403



Internal ID16032126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:122181001..122215314hg38UCSC Ensembl
Innerchr3:121899848..121934161hg19UCSC Ensembl
Innerchr3:123382538..123416851hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3834314
hg1934314
hg1834314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8526n54
Supporting Variantsnssv971768
Samples
Known GenesCASR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591403
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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