A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016800



Internal ID21926143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97193141..97193297hg38UCSC Ensembl
chr10:98952898..98953054hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582215
Samples
Known GenesARHGAP19-SLIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016800
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