A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597958



Internal ID21790002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34464488..34470387hg38UCSC Ensembl
chr14:34933694..34939593hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039706
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597958
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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