A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083526



Internal ID21278472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19175508..19180462hg38UCSC Ensembl
Innerchr6:19175739..19180693hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384955
hg194955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115884
Supporting Variants
Samplessample27
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083526
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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