A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891531



Internal ID22666571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26711068..27072879hg38UCSC Ensembl
chr4:26712690..27074501hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38361812
hg19361812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414213
Samples
Known GenesSTIM2, TBC1D19
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891531
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