A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078661



Internal ID21987894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166997813..166997813hg38UCSC Ensembl
chr6:167411301..167411301hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381411
hg191411
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565705
Samples
Known GenesMIR3939
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078661
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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