A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378786



Internal ID22436656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83885245..83885319hg38UCSC Ensembl
chr14:84351589..84351663hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378786
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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