A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913277



Internal ID22688493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31845756..31854403hg38UCSC Ensembl
chr10:32134684..32143331hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg388648
hg198648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365663
Samples
Known GenesARHGAP12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913277
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