A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071484



Internal ID21980717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30246624..30246624hg38UCSC Ensembl
chr8:30104140..30104140hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575741
Samples
Known GenesMIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071484
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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