A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028233



Internal ID21937576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38439074..38439138hg38UCSC Ensembl
chr17:36595319..36595383hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626792
Samples
Known GenesARHGAP23
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028233
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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