A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438719



Internal ID21096272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5537833..5547160hg38UCSC Ensembl
chr11:5559063..5568390hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg389328
hg199328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992219
Samples
Known GenesOR52H1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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