A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022228



Internal ID21931571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76190698..76191382hg38UCSC Ensembl
chr17:74186779..74187463hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38685
hg19685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617787
Samples
Known GenesRNF157
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022228
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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