A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18108859



Internal ID20675899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145113698..145114332hg38UCSC Ensembl
chr4:146034850..146035484hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389300
Supporting Variants
Samples
Known GenesABCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18108859
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