A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18070495



Internal ID20637535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7718401..7720900hg38UCSC Ensembl
chr20:7699048..7701547hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523601
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18070495
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00126


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