A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462088



Internal ID21119641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118848096..118861795hg38UCSC Ensembl
chr11:118718805..118732504hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3813700
hg1913700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462088
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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