A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182143



Internal ID20749183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26055801..26060300hg38UCSC Ensembl
chr15:26300948..26305447hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182143
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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