A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438956



Internal ID21096509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22124501..22125400hg38UCSC Ensembl
chr11:22146047..22146946hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989514
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438956
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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