A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373051



Internal ID22598720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82617880..82634979hg38UCSC Ensembl
chr14:83084224..83101323hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3817100
hg1917100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373051
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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