A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177847



Internal ID20744887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34329701..34561700hg38UCSC Ensembl
chr15:34621902..34853901hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38232000
hg19232000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497589
Supporting Variants
Samples
Known GenesGOLGA8A, GOLGA8B, LPCAT4, MIR1233-1, MIR1233-2, NOP10, NUTM1, SLC12A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177847
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00021


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