A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069847



Internal ID20636887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:20154957..20158414hg38UCSC Ensembl
chr21:21527270..21530727hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg383458
hg193458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538689
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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