A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486689



Internal ID21144242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83500201..83578000hg38UCSC Ensembl
chr13:84074336..84152135hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3877800
hg1977800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486689
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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