A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082992



Internal ID21282721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:155103151..155107772hg38UCSC Ensembl
Innerchr6:155424285..155428906hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg384622
hg194622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117900
Supporting Variants
Samplessample331
Known GenesTIAM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082992
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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