A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294056



Internal ID20503274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155954565..155954565hg38UCSC Ensembl
chr1:155924356..155924356hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764546
Supporting Variants
Samples
Known GenesARHGEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294056
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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