A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472554



Internal ID21130107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107558116..107558535hg38UCSC Ensembl
chr11:107428842..107429261hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986555
Samples
Known GenesALKBH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472554
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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