A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441415



Internal ID21098968
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 StatusM
Merged Variants
Supporting Variantsnssv18193445
Samples
Known GenesKCNC1, MYOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441415
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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