A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615997



Internal ID21808044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56576930..56577138hg38UCSC Ensembl
chr14:57043648..57043856hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040094
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615997
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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