A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317669



Internal ID20850757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:164588915..164590173hg38UCSC Ensembl
chr1:164558152..164559410hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg381259
hg191259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052788
Samples
Known GenesPBX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317669
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