A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592362



Internal ID16033085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163001200..163003875hg38UCSC Ensembl
Innerchr3:162718988..162721663hg19UCSC Ensembl
Innerchr3:164201682..164204357hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg382676
hg192676
hg182676
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8701n54
Supporting Variantsnssv979343, nssv979323, nssv979330, nssv979338, nssv979340, nssv979337, nssv979332, nssv979324, nssv979342, nssv979334, nssv979333, nssv979327, nssv979339, nssv979326, nssv979341, nssv979336, nssv979335, nssv979325, nssv979331, nssv979328, nssv979329
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592362
Frequency
Sample Size17421
Observed Gain13
Observed Loss8
Observed Complex0
Frequencyn/a


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