A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490165



Internal ID21147718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39167925..39188797hg38UCSC Ensembl
chr13:39742062..39762934hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3820873
hg1920873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490165
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