A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497589



Internal ID20870797
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 StatusM
Merged Variantsdgv2487n223
Supporting Variantsnssv18177847
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)nsv6497589
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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