A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041522



Internal ID21950855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155964206..155964206hg38UCSC Ensembl
chr1:155933997..155933997hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530117
Samples
Known GenesARHGEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041522
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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