A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438088



Internal ID21095641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1303040..1410027hg38UCSC Ensembl
chr11:1324270..1431257hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38106988
hg19106988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184405
Samples
Known GenesBRSK2, TOLLIP, TOLLIP-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438088
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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