A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032993



Internal ID20600033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84393921..84395795hg38UCSC Ensembl
chr16:84427527..84429401hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381875
hg191875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499729
Supporting Variants
Samples
Known GenesATP2C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032993
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00145


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