A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320390



Internal ID20853488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159186250..159186612hg38UCSC Ensembl
chr1:159156040..159156402hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053502
Samples
Known GenesCADM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320390
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