A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539823



Internal ID20913118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38520575..38529158hg38UCSC Ensembl
chr22:38916580..38925163hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg388584
hg198584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073980
Samples
Known GenesDMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539823
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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