A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497524



Internal ID22555458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9824894..9829755hg38UCSC Ensembl
chr3:9866578..9871439hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg384862
hg194862
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836922
Supporting Variants
Samples
Known GenesARPC4-TTLL3, TTLL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497524
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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