A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459006



Internal ID21116559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62654030..62659015hg38UCSC Ensembl
chr11:62421502..62426487hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg384986
hg194986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993219
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459006
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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