A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465793



Internal ID21123346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98876689..98947110hg38UCSC Ensembl
chr11:98747419..98817840hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3870422
hg1970422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996486
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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