A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485849



Internal ID21143402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51088404..51094871hg38UCSC Ensembl
chr13:51662540..51669007hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg386468
hg196468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009653
Samples
Known GenesLINC00371
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485849
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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