A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452846



Internal ID21110399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8365060..8372737hg38UCSC Ensembl
chr11:8386607..8394284hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387678
hg197678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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