A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481953



Internal ID21139506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107349428..107661665hg38UCSC Ensembl
chr13:108001776..108314013hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38312238
hg19312238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006407
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481953
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