A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233260



Internal ID20800300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:87884767..87897161hg38UCSC Ensembl
chr8:88896995..88909389hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3812395
hg1912395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432653
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233260
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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