A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072029



Internal ID20639069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29492001..29493100hg38UCSC Ensembl
chr21:30864321..30865420hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540405
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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