A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497637



Internal ID20870845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43470901..43478100hg38UCSC Ensembl
chr15:43763099..43770298hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179368
Samples
Known GenesRNU6-28P, TP53BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497637
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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