A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591930



Internal ID16379339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144433380..144461734hg38UCSC Ensembl
Innerchr3:144152222..144180576hg19UCSC Ensembl
Innerchr3:145634912..145663266hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3828355
hg1928355
hg1828355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv975230
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591930
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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