A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262071



Internal ID20471289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12862811..12863103hg38UCSC Ensembl
chr17:12766128..12766420hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731888
Supporting Variants
Samples
Known GenesARHGAP44
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262071
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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