A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965407



Internal ID18253955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46754541..46808658hg38UCSC Ensembl
Innerchr3:46796031..46850148hg19UCSC Ensembl
Innerchr3:46771035..46825152hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3854118
hg1954118
hg1854118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2757017, nssv2763827, nssv2758739, nssv2757446
SamplesHGDP01284, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965407
Frequency
Sample Size10
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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