A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408946



Internal ID21066499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93587301..93589000hg38UCSC Ensembl
chr5:92923007..92924706hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215018
Samples
Known GenesMIR548AO, NR2F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408946
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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