A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096798



Internal ID21289194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:52672151..52673577hg38UCSC Ensembl
Innerchr5:51967985..51969411hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381427
hg191427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115397
Supporting Variants
Samplessample44
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096798
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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