A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383394



Internal ID22441264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103596062..103601167hg38UCSC Ensembl
chr14:104062399..104067504hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg385106
hg195106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383394
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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