A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083918



Internal ID21287767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3216492..3223653hg38UCSC Ensembl
Innerchr6:3216726..3223887hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg387162
hg197162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113641
Supporting Variants
Samplessample407
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083918
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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