A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236137



Internal ID20803177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:112915901..112978700hg38UCSC Ensembl
chr8:113928130..113990929hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3862800
hg1962800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433078
Supporting Variants
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236137
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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