A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072202



Internal ID21981435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75167893..75167893hg38UCSC Ensembl
chr8:76080128..76080128hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072202
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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