A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469053



Internal ID21126606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45359862..45362646hg38UCSC Ensembl
chr11:45381413..45384197hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382785
hg192785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991701
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469053
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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