A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072803



Internal ID20639843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45581781..45582070hg38UCSC Ensembl
chr21:47001695..47001984hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00242


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