A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693441



Internal ID117107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24435710..24435874hg38UCSC Ensembl
chr14:24904916..24905080hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5508754
Supporting Variants
Samples
Known GenesKHNYN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693441
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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