A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086299



Internal ID21267854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64148773..64294712hg38UCSC Ensembl
Innerchr6:64858666..65004605hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38145940
hg19145940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118029
Supporting Variants
Samplessample117
Known GenesEYS
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086299
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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