A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465515



Internal ID21123068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41377265..41465823hg38UCSC Ensembl
chr11:41398815..41487373hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3888559
hg1988559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189479
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465515
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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