A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033081



Internal ID20600121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85050560..85053090hg38UCSC Ensembl
chr16:85084166..85086696hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382531
hg192531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497559
Supporting Variants
Samples
Known GenesKIAA0513
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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