A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050985



Internal ID21960219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3475499..3475499hg38UCSC Ensembl
chr1:3392063..3392063hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520810
Samples
Known GenesARHGEF16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050985
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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