A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512551



Internal ID20885886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52247813..52256588hg38UCSC Ensembl
chr15:52540010..52548785hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg388776
hg198776
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189053
Samples
Known GenesMYO5C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512551
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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