A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944398



Internal ID22719862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101692693..101693380hg38UCSC Ensembl
chr14:102159030..102159717hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944398
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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