A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591924



Internal ID16379333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144057254..144145938hg38UCSC Ensembl
Innerchr3:143776096..143864780hg19UCSC Ensembl
Innerchr3:145258786..145347470hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3888685
hg1988685
hg1888685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8627n54
Supporting Variantsnssv975223
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591924
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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