A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477404



Internal ID21134957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112953201..112955900hg38UCSC Ensembl
chr13:113607515..113610214hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185483
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477404
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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