A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607967



Internal ID21800014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70580454..70582572hg38UCSC Ensembl
chr14:71047171..71049289hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg382119
hg192119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029020
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607967
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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