A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599524



Internal ID21791569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51911625..51912184hg38UCSC Ensembl
chr14:52378343..52378902hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036012
Supporting Variants
Samples
Known GenesGNG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599524
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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