A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17042090



Internal ID95761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2621066..2621127hg38UCSC Ensembl
chr11:2642296..2642357hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503194
Supporting Variants
Samples
Known GenesKCNQ1, KCNQ1OT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17042090
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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