A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019162



Internal ID20586202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51980096..51983562hg38UCSC Ensembl
chr14:52446814..52450280hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg383467
hg193467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00051


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