A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169707



Internal ID20736747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59579901..59580800hg38UCSC Ensembl
chr8:60492460..60493359hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425977
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00061


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