A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203949



Internal ID20770989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38193998..38206776hg38UCSC Ensembl
chr21:39566092..39578870hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3812779
hg1912779
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539604
Supporting Variants
Samples
Known GenesDSCR10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203949
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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