A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204248



Internal ID20771288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9823312..9837379hg38UCSC Ensembl
chr4_gl000193_random:90626..104693hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3814068
hg1914068
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549856
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204248
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00846


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