A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372926



Internal ID22598595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81817246..81817532hg38UCSC Ensembl
chr14:82283590..82283876hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942612
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372926
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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