A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181471



Internal ID20748511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30988401..30996400hg38UCSC Ensembl
chr15:31280604..31288603hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499391
Supporting Variants
Samples
Known GenesMTMR10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181471
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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