A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082921



Internal ID21281565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:142088705..142091846hg38UCSC Ensembl
Innerchr6:142409842..142412983hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg383142
hg193142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115230
Supporting Variants
Samplessample313
Known GenesNMBR
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082921
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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