A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18070362



Internal ID20637402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7084301..7085200hg38UCSC Ensembl
chr20:7064948..7065847hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528735
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18070362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00056


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