A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473192



Internal ID21130745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40460389..40474140hg38UCSC Ensembl
chr11:40481939..40495690hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3813752
hg1913752
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185702
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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