A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416426



Internal ID22474296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26644925..26645006hg38UCSC Ensembl
chr4:26646547..26646628hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897166
Supporting Variants
Samples
Known GenesTBC1D19
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416426
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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