A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490907



Internal ID21148460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49970723..49983249hg38UCSC Ensembl
chr13:50544859..50557385hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3812527
hg1912527
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193504
Samples
Known GenesDLEU2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490907
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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