A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990559



Internal ID20557600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3790073..3791065hg38UCSC Ensembl
chr11:3811303..3812295hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38993
hg19993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442032
Supporting Variants
Samples
Known GenesNUP98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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