A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356569



Internal ID21014122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101969464..101980297hg38UCSC Ensembl
chr3:101688308..101699141hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3810834
hg1910834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092434
Samples
Known GenesLOC152225
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356569
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