A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194462



Internal ID20761502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125266329..125268732hg38UCSC Ensembl
chr10:126954898..126957301hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382404
hg192404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446092
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194462
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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