A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014337



Internal ID21923680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100821620..100936907hg38UCSC Ensembl
chr8:101833848..101949135hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38115288
hg19115288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592637
Samples
Known GenesYWHAZ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014337
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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