A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033078



Internal ID20600118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85025085..85030485hg38UCSC Ensembl
chr16:85058691..85064091hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385401
hg195401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505082
Supporting Variants
Samples
Known GenesKIAA0513
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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