A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070400



Internal ID21979633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102080221..102080221hg38UCSC Ensembl
chr8:103092449..103092449hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580824
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070400
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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