A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015600



Internal ID21924943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:14021032..14206101hg38UCSC Ensembl
chr8:13878541..14063610hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38185070
hg19185070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576495
Samples
Known GenesSGCZ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015600
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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