A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445561



Internal ID21103114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3828601..3830000hg38UCSC Ensembl
chr11:3849831..3851230hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991637
Samples
Known GenesRHOG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445561
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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