A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207544



Internal ID20774584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44146081..44146334hg38UCSC Ensembl
chr22:44541961..44542214hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549381
Supporting Variants
Samples
Known GenesPARVB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207544
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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