A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477449



Internal ID21135002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113592701..113594600hg38UCSC Ensembl
chr13:114247016..114248915hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177384, nssv18007775
Samples
Known GenesTFDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477449
Frequency
Sample Size19652
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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