A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989926



Internal ID20556966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3662093..3669077hg38UCSC Ensembl
chr11:3683323..3690307hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386985
hg196985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452909
Supporting Variants
Samples
Known GenesART1, CHRNA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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