A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015725



Internal ID21925068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42852490..42852597hg38UCSC Ensembl
chr8:42707633..42707740hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581324
Samples
Known GenesRNF170
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015725
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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