A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061557



Internal ID21970790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27745159..27745159hg38UCSC Ensembl
chr8:27602676..27602676hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565499
Samples
Known GenesCCDC25
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061557
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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