A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592370



Internal ID16033093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163001313..163003460hg38UCSC Ensembl
Innerchr3:162719101..162721248hg19UCSC Ensembl
Innerchr3:164201795..164203942hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg382148
hg192148
hg182148
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8701n54
Supporting Variantsnssv979815, nssv979809, nssv979811, nssv979813, nssv979812, nssv979810, nssv979807, nssv979808, nssv979814
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592370
Frequency
Sample Size17421
Observed Gain8
Observed Loss1
Observed Complex0
Frequencyn/a


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