A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400980



Internal ID21058533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95061498..95072808hg38UCSC Ensembl
chr5:94397202..94408512hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3811311
hg1911311
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215024
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400980
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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