A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495340



Internal ID21152893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:65181713..65217320hg38UCSC Ensembl
chr13:65755845..65791452hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3835608
hg1935608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193074
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495340
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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