A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992838



Internal ID20559878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7063035..7068805hg38UCSC Ensembl
chr11:7084266..7090036hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385771
hg195771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440509
Supporting Variants
Samples
Known GenesNLRP14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992838
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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