A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042428



Internal ID21951744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107723537..107723537hg38UCSC Ensembl
chr1:108266159..108266159hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381838
hg191838
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530979
Samples
Known GenesVAV3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042428
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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