A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182598



Internal ID20749638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48623769..48638787hg38UCSC Ensembl
chr10:49831814..49846832hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3815019
hg1915019
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455098
Supporting Variants
Samples
Known GenesARHGAP22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182598
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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