A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086482



Internal ID21270579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137649768..137660359hg38UCSC Ensembl
Innerchr6:137970905..137981496hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3810592
hg1910592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110324
Supporting Variants
Samplessample152
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086482
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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