A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070332



Internal ID21979565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126335584..126335584hg38UCSC Ensembl
chr6:126656730..126656730hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070332
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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