A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194955



Internal ID20761995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41313417..41473126hg38UCSC Ensembl
chr15:41605615..41765324hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38159710
hg19159710
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513499
Supporting Variants
Samples
Known GenesNDUFAF1, NUSAP1, OIP5, RTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194955
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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