A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083524



Internal ID21277856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103463588..103500590hg38UCSC Ensembl
Innerchr6:103911463..103948465hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3837003
hg1937003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117100
Supporting Variants
Samplessample26
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083524
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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