A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413146



Internal ID21070699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95163284..95328152hg38UCSC Ensembl
chr5:94498988..94663856hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38164869
hg19164869
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215026
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413146
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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