A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066793



Internal ID21976026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97224947..97224947hg38UCSC Ensembl
chr6:97672823..97672823hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558982
Samples
Known GenesMIR548H3, MMS22L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066793
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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