A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229573



Internal ID20796613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:134826301..134831700hg38UCSC Ensembl
chr8:135838544..135843943hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432047
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229573
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00089


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