A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897166



Internal ID22672265
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 StatusM
Merged Variants
Supporting Variantsnssv17416426
Samples
Known GenesTBC1D19
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897166
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