A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477980



Internal ID21135533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31938701..31968100hg38UCSC Ensembl
chr13:32512838..32542237hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3829400
hg1929400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189415
Samples
Known GenesEEF1DP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477980
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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