A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388326



Internal ID22446196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92194707..92198457hg38UCSC Ensembl
chr14:92661051..92664801hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg383751
hg193751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945321
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388326
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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