A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002197



Internal ID21911540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53593978..53594072hg38UCSC Ensembl
chr8:54506538..54506632hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002197
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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