A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922764



Internal ID22697989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97162616..97162943hg38UCSC Ensembl
chr10:98922373..98922700hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355579
Samples
Known GenesARHGAP19-SLIT1, SLIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922764
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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