A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475417



Internal ID21132970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99155412..99211488hg38UCSC Ensembl
chr11:99026143..99082219hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3856077
hg1956077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188087
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475417
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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