A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031440



Internal ID20598480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74834683..74957866hg38UCSC Ensembl
chr16:74868581..74991764hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38123184
hg19123184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503156
Supporting Variants
Samples
Known GenesWDR59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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