A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028794



Internal ID20595834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2345266..2352340hg38UCSC Ensembl
chr16:2395267..2402341hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg387075
hg197075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497728
Supporting Variants
Samples
Known GenesABCA17P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028794
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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