A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547998



Internal ID20921197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40897192..40902511hg38UCSC Ensembl
chr22:41293196..41298515hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg385320
hg195320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206807
Samples
Known GenesXPNPEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547998
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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