A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183296



Internal ID20750336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41297432..41311400hg38UCSC Ensembl
chr15:41589630..41603598hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3813969
hg1913969
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500534
Supporting Variants
Samples
Known GenesOIP5, OIP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183296
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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