A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083376



Internal ID21292969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2844779..2853161hg38UCSC Ensembl
Innerchr7:2884413..2892795hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg388383
hg198383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114977
Supporting Variants
Samplessample94
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083376
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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