A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374169



Internal ID22599838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53158566..53159114hg38UCSC Ensembl
chr14:53625284..53625832hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930820
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374169
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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