A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699501



Internal ID123167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93141411..93162232hg38UCSC Ensembl
chr14:93607756..93628577hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3820822
hg1920822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500330
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699501
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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