A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032978



Internal ID20600018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84293079..84419646hg38UCSC Ensembl
chr16:84326685..84453252hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38126568
hg19126568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505274
Supporting Variants
Samples
Known GenesATP2C2, WFDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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