A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831023



Internal ID22605958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143164128..143171551hg38UCSC Ensembl
chr2:143921697..143929120hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg387424
hg197424
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487723
Samples
Known GenesARHGAP15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831023
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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