A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203941



Internal ID20770981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36625427..36634245hg38UCSC Ensembl
chr21:37997725..38006543hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg388819
hg198819
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203941
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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