A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486017



Internal ID21143570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74369575..74448225hg38UCSC Ensembl
chr13:74943712..75022362hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3878651
hg1978651
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192383
Samples
Known GenesLINC00381
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486017
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer