A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107521



Internal ID20674562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103083798..103084424hg38UCSC Ensembl
chr4:104004955..104005581hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387942
Supporting Variants
Samples
Known GenesBDH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107521
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