A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452997



Internal ID21110550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1316118..1316918hg38UCSC Ensembl
chr11:1337348..1338148hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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