A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477129



Internal ID21134682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82713112..82716175hg38UCSC Ensembl
chr13:83287247..83290310hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg383064
hg193064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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