A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193445



Internal ID20760485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17708484..17750480hg38UCSC Ensembl
chr11:17730031..17772027hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3841997
hg1941997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441415
Supporting Variants
Samples
Known GenesKCNC1, MYOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193445
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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