A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028938



Internal ID20595978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31199618..31224465hg38UCSC Ensembl
chr16:31210939..31235786hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3824848
hg1924848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496584
Supporting Variants
Samples
Known GenesC16orf98, PYCARD, PYDC1, TRIM72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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