A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012966



Internal ID18755497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46750043..46818330hg38UCSC Ensembl
Innerchr3:46791533..46859820hg19UCSC Ensembl
Innerchr3:46766537..46834824hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3868288
hg1968288
hg1868288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4732n100
Supporting Variantsnssv3590919, nssv3590917, nssv3590918
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)nsv1012966
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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