A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591977



Internal ID16379386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149235238..149248900hg38UCSC Ensembl
Innerchr3:148953025..148966687hg19UCSC Ensembl
Innerchr3:150435715..150449377hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3813663
hg1913663
hg1813663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8637n54
Supporting Variantsnssv976389
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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