A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064162



Internal ID21973395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97619096..97619096hg38UCSC Ensembl
chr8:98631324..98631324hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg383709
hg193709
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593994
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064162
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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