A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042692



Internal ID21952004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235309370..235309370hg38UCSC Ensembl
chr1:235472685..235472685hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517587
Samples
Known GenesARID4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042692
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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