A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370674



Internal ID21028227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72962758..72965138hg38UCSC Ensembl
chr3:73011909..73014289hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382381
hg192381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103819
Samples
Known GenesGXYLT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370674
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