A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994444



Internal ID20561484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8429018..8431780hg38UCSC Ensembl
chr11:8450565..8453327hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382763
hg192763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439475
Supporting Variants
Samples
Known GenesSTK33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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