A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015606



Internal ID20582646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101650458..101650830hg38UCSC Ensembl
chr14:102116795..102117167hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498590
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00048


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