A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071893



Internal ID21981126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90080489..90080489hg38UCSC Ensembl
chr8:91092717..91092717hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578828
Samples
Known GenesCALB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071893
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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