A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990811



Internal ID20557851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3388301..3390800hg38UCSC Ensembl
chr11:3409531..3412030hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443052
Supporting Variants
Samples
Known GenesLOC650368, OR7E12P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990811
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00169


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