A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072598



Internal ID21981831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29771253..29771253hg38UCSC Ensembl
chr8:29628769..29628769hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577403
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072598
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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