A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060402



Internal ID20627442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31744960..31746076hg38UCSC Ensembl
chr1:32210561..32211677hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg381117
hg191117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317589
Supporting Variants
Samples
Known GenesBAI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer