A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061850



Internal ID20628890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57495369..57495807hg38UCSC Ensembl
chr1:57961041..57961479hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331717
Supporting Variants
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061850
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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