A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374649



Internal ID22600318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45865298..45930672hg38UCSC Ensembl
chr14:46334501..46399875hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3865375
hg1965375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374649
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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