A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602440



Internal ID21794487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34659524..34659589hg38UCSC Ensembl
chr14:35128730..35128795hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602440
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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