A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592360



Internal ID16033083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163001200..163003460hg38UCSC Ensembl
Innerchr3:162718988..162721248hg19UCSC Ensembl
Innerchr3:164201682..164203942hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg382261
hg192261
hg182261
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8701n54
Supporting Variantsnssv979306, nssv979302, nssv979312, nssv979294, nssv979307, nssv979304, nssv979292, nssv979298, nssv979309, nssv979314, nssv979315, nssv979313, nssv979310, nssv979317, nssv979301, nssv979300, nssv979296, nssv979311, nssv979297, nssv979299, nssv979305, nssv979316, nssv979303, nssv979295, nssv979308, nssv979293
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592360
Frequency
Sample Size17421
Observed Gain12
Observed Loss14
Observed Complex0
Frequencyn/a


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