A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031450



Internal ID20598490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74978149..74984007hg38UCSC Ensembl
chr16:75012047..75017905hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg385859
hg195859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513646
Supporting Variants
Samples
Known GenesWDR59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031450
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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