A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375772



Internal ID22601441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105742107..105773688hg38UCSC Ensembl
chr14:106208444..106240025hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3831582
hg1931582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375772
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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