A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490161



Internal ID21147714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56832101..56934600hg38UCSC Ensembl
chr13:57406235..57508734hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38102500
hg19102500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185505
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490161
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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