A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011442



Internal ID18753976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46807779hg38UCSC Ensembl
Innerchr3:46801805..46849269hg19UCSC Ensembl
Innerchr3:46776809..46824273hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3847465
hg1947465
hg1847465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3601546, nssv3601542, nssv3601558, nssv3601559, nssv3601547, nssv3601544, nssv3601548, nssv3601556, nssv3739738, nssv3601554, nssv3601549, nssv3601555, nssv3601552, nssv3601553, nssv3601550, nssv3601540, nssv3739737, nssv3601551, nssv3601543, nssv3601557, nssv3601545, nssv3601541
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011442
Frequency
Sample Size29084
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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