A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369320



Internal ID22594989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24588347..24588422hg38UCSC Ensembl
chr10:24877276..24877351hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916624
Supporting Variants
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369320
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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