A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008356



Internal ID21917699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9771124..9772104hg38UCSC Ensembl
chr8:9628634..9629614hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38981
hg19981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568734
Samples
Known GenesTNKS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008356
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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