A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203024



Internal ID20770064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:13122301..13374500hg38UCSC Ensembl
chr21:14494622..14746821hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38252200
hg19252200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539952
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203024
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0009


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