A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462566



Internal ID21120119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124191249..124191624hg38UCSC Ensembl
chr11:124061956..124062331hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987792
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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