A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472579



Internal ID21130132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119795102..119795947hg38UCSC Ensembl
chr11:119665811..119666656hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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