A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471613



Internal ID21129166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123691112..123691897hg38UCSC Ensembl
chr11:123561820..123562605hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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