A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507845



Internal ID20881141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62220975..62849523hg38UCSC Ensembl
chr15:62513174..63141722hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38628549
hg19628549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185824
Samples
Known GenesMGC15885, MIR190A, MIR6085, MIR8067, TLN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507845
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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