A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010209



Internal ID21919552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70287653..70331147hg38UCSC Ensembl
chr8:71199888..71243382hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3843495
hg1943495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592541
Samples
Known GenesNCOA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010209
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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