A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082977



Internal ID21282497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121640345..121649466hg38UCSC Ensembl
Innerchr6:121961491..121970612hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg389122
hg199122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116731
Supporting Variants
Samplessample328
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082977
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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