A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098239



Internal ID22007472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97251786..97251786hg38UCSC Ensembl
chr10:99011543..99011543hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588921
Samples
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098239
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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