A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083776



Internal ID21292087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74687558..74701243hg38UCSC Ensembl
Innerchr6:75397274..75410959hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3813686
hg1913686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113822
Supporting Variants
Samplessample82
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083776
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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