A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577579



Internal ID21769622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2464756..2474616hg38UCSC Ensembl
chr11:2485986..2495846hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg389861
hg199861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034165
Supporting Variants
Samples
Known GenesKCNQ1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577579
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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