A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592382



Internal ID16033105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163001459..163003684hg38UCSC Ensembl
Innerchr3:162719247..162721472hg19UCSC Ensembl
Innerchr3:164201941..164204166hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg382226
hg192226
hg182226
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8701n54
Supporting Variantsnssv979862, nssv979863
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592382
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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