A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069849



Internal ID21979082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142963163..142963163hg38UCSC Ensembl
chr5:142342728..142342728hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548794
Samples
Known GenesARHGAP26
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069849
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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