A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224199



Internal ID20791239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81520601..81524800hg38UCSC Ensembl
chr8:82432836..82437035hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418601
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224199
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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