A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016628



Internal ID20583668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20932145..20958230hg38UCSC Ensembl
chr14:21400304..21426389hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3826086
hg1926086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489490
Supporting Variants
Samples
Known GenesRNASE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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