A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511648



Internal ID20884978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94008168..94813217hg38UCSC Ensembl
chr15:94551397..95356446hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38805050
hg19805050
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183025
Samples
Known GenesMCTP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511648
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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