A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470099



Internal ID21127652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86196598..86197258hg38UCSC Ensembl
chr11:85907640..85908300hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994600
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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