A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700566



Internal ID124232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105008665..105008959hg38UCSC Ensembl
chr14:105475002..105475296hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700566
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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