A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463841



Internal ID21121394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81725234..81859793hg38UCSC Ensembl
chr11:81436276..81570835hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38134560
hg19134560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463841
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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