A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410016



Internal ID22467886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85520065..85520065hg38UCSC Ensembl
chr4:86441218..86441218hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954508
Supporting Variants
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410016
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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