A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493329



Internal ID21150882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38960898..39169443hg38UCSC Ensembl
chr13:39535035..39743580hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38208546
hg19208546
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195928
Samples
Known GenesNHLRC3, PROSER1, STOML3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493329
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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