A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478799



Internal ID21136352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36151501..36156900hg38UCSC Ensembl
chr13:36725638..36731037hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478799
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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