A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841664



Internal ID22025307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48514662..48514662hg38UCSC Ensembl
chr10:49722705..49722705hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240640
Supporting Variants
Samples
Known GenesARHGAP22
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841664
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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