A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191231



Internal ID20758271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79886801..79941800hg38UCSC Ensembl
chr15:80179143..80234142hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3855000
hg1955000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498380
Supporting Variants
Samples
Known GenesC15orf37, MTHFS, ST20, ST20-MTHFS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191231
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00056


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