A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462379



Internal ID21119932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127205342..127205818hg38UCSC Ensembl
chr11:127075237..127075713hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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