A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400896



Internal ID21058449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77766801..77799800hg38UCSC Ensembl
chr5:77062625..77095624hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3833000
hg1933000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214146
Samples
Known GenesTBCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400896
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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