A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501354



Internal ID20874587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62723399..62892082hg38UCSC Ensembl
chr15:63015598..63184281hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38168684
hg19168684
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185074
Samples
Known GenesMIR190A, TLN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501354
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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