A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059728



Internal ID21968961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241878213..241878213hg38UCSC Ensembl
chr1:242041515..242041515hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530599
Samples
Known GenesEXO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059728
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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