A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550943



Internal ID20924086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39299086..39303076hg38UCSC Ensembl
chr22:39695091..39699081hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383991
hg193991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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