A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103044



Internal ID21279979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35446177..35452488hg38UCSC Ensembl
Innerchr22:35842170..35848481hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg386312
hg196312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117305
Supporting Variants
Samplessample291
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103044
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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