A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990287



Internal ID20557328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30016801..30017400hg38UCSC Ensembl
chr11:30038348..30038947hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438838
Supporting Variants
Samples
Known GenesKCNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01317


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