A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192860



Internal ID20759900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41392309..41406202hg38UCSC Ensembl
chr15:41684507..41698400hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3813894
hg1913894
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498960
Supporting Variants
Samples
Known GenesNDUFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192860
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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