A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018564



Internal ID21927907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25346559..25346784hg38UCSC Ensembl
chr8:25204075..25204300hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568685
Samples
Known GenesDOCK5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018564
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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