A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988703



Internal ID20555743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19159517..19161734hg38UCSC Ensembl
chr11:19181064..19183281hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382218
hg192218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440973
Supporting Variants
Samples
Known GenesZDHHC13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988703
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00475


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