A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401416



Internal ID21058969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95134928..95139148hg38UCSC Ensembl
chr5:94470632..94474852hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg384221
hg194221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215025
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401416
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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