A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479691



Internal ID21137244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33558661..33564775hg38UCSC Ensembl
chr13:34132798..34138912hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg386115
hg196115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008781
Samples
Known GenesSTARD13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479691
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