A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608029



Internal ID21800076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35087574..35269684hg38UCSC Ensembl
chr14:35556780..35738890hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38182111
hg19182111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036383
Supporting Variants
Samples
Known GenesKIAA0391, PPP2R3C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608029
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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