A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087779



Internal ID21276411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139279829..139285895hg38UCSC Ensembl
Innerchr6:139600966..139607032hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg386067
hg196067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115983
Supporting Variants
Samplessample236
Known GenesTXLNB
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087779
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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