A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073836



Internal ID20640876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40540046..40545546hg38UCSC Ensembl
chr22:40936050..40941550hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385501
hg195501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549225
Supporting Variants
Samples
Known GenesMKL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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