A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001314



Internal ID21910657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85273548..85273622hg38UCSC Ensembl
chr8:86185777..86185851hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595927
Samples
Known GenesCA13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001314
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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