A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611291



Internal ID21803338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35977513..35977689hg38UCSC Ensembl
chr14:36446719..36446895hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027494
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611291
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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