A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694983



Internal ID118649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41002828..41016477hg38UCSC Ensembl
chr14:41472033..41485682hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3813650
hg1913650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5508233
Supporting Variants
Samples
Known GenesLOC644919
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694983
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003435


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