A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072770



Internal ID21982003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125592268..125592268hg38UCSC Ensembl
chr6:125913414..125913414hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382313
hg192313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575710
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072770
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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