A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206386



Internal ID20773426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63065888..63066331hg38UCSC Ensembl
chr2:63293023..63293466hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6336865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206386
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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