A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224862



Internal ID20791902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55464483..55480408hg38UCSC Ensembl
chr8:56377043..56392968hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3815926
hg1915926
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425409
Supporting Variants
Samples
Known GenesXKR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224862
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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