A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231411



Internal ID20798451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67108437..67137151hg38UCSC Ensembl
chr8:68020672..68049386hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3828715
hg1928715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423324
Supporting Variants
Samples
Known GenesCSPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231411
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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