A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230407



Internal ID20797447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41262302..41410732hg38UCSC Ensembl
chr8:41119821..41268251hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38148431
hg19148431
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421486
Supporting Variants
Samples
Known GenesSFRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230407
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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