A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029975



Internal ID20597015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4939855..5080204hg38UCSC Ensembl
chr16:4989856..5130205hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38140350
hg19140350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509683
Supporting Variants
Samples
Known GenesALG1, C16orf89, NAGPA, NAGPA-AS1, SEC14L5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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