A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496928



Internal ID20870131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63411453..63569726hg38UCSC Ensembl
chr15:63703652..63861925hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38158274
hg19158274
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183940
Samples
Known GenesUSP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496928
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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