A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491399



Internal ID21148952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101411101..101416100hg38UCSC Ensembl
chr13:102063452..102068451hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180971
Samples
Known GenesNALCN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491399
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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