A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177263



Internal ID20744303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28452401..28753200hg38UCSC Ensembl
chr15:28697547..28998346hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38300800
hg19300800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509503
Supporting Variants
Samples
Known GenesGOLGA8F, GOLGA8G, GOLGA8M, HERC2P9, MIR4509-1, MIR4509-2, MIR4509-3, WHAMMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177263
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00062


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