A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229829



Internal ID20796870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83089501..83883500hg38UCSC Ensembl
chr8:84001736..84795735hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38794000
hg19794000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229829
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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