A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224106



Internal ID20791146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76405847..76426526hg38UCSC Ensembl
chr8:77318082..77338761hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3820680
hg1920680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433945
Supporting Variants
Samples
Known GenesLINC01111
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224106
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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