A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505933



Internal ID20879207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52053250..52053814hg38UCSC Ensembl
chr15:52345447..52346011hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179474
Samples
Known GenesMAPK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505933
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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