A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377603



Internal ID22435473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97663688..97674611hg38UCSC Ensembl
chr14:98130025..98140948hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3810924
hg1910924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935392
Supporting Variants
Samples
Known GenesLOC100129345
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377603
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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