A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455170



Internal ID21112723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1135601..1143700hg38UCSC Ensembl
chr11:1129509..1137608hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388100
hg198100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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