A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367304



Internal ID22592973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155956539..155956808hg38UCSC Ensembl
chr1:155926330..155926599hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871617
Supporting Variants
Samples
Known GenesARHGEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367304
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