A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466973



Internal ID22524865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:44924229..44925885hg38UCSC Ensembl
chr14:45393432..45395088hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg381657
hg191657
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849084
Supporting Variants
Samples
Known GenesKLHL28
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466973
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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