A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387645



Internal ID22445515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49880266..49891913hg38UCSC Ensembl
chr14:50346984..50358631hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3811648
hg1911648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935211
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387645
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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