A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187626



Internal ID20754666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41326682..41460753hg38UCSC Ensembl
chr15:41618880..41752951hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38134072
hg19134072
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511818
Supporting Variants
Samples
Known GenesNDUFAF1, NUSAP1, OIP5, RTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187626
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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