A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598439



Internal ID21790484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20763259..20767522hg38UCSC Ensembl
chr14:21231418..21235681hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg384264
hg194264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025810
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598439
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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