A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590181



Internal ID16030904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46754860..46807583hg38UCSC Ensembl
Innerchr3:46796350..46849073hg19UCSC Ensembl
Innerchr3:46771354..46824077hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3852724
hg1952724
hg1852724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8304n54
Supporting Variantsnssv962496, nssv962509, nssv962499, nssv962508, nssv962486, nssv962517, nssv962495, nssv962497, nssv962511, nssv962491, nssv962493, nssv962507, nssv962515, nssv962488, nssv962503, nssv962513, nssv962489, nssv962510, nssv962502, nssv962518, nssv962512, nssv962498, nssv962487, nssv962490, nssv962514, nssv962504, nssv962519, nssv962501, nssv962506, nssv962516, nssv962492, nssv962494, nssv962500, nssv962505
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590181
Frequency
Sample Size17421
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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