A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480792



Internal ID21138345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113593642..113594601hg38UCSC Ensembl
chr13:114247957..114248916hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196257
Samples
Known GenesTFDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480792
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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