A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620107



Internal ID21812154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5367551..5368026hg38UCSC Ensembl
chr17:5270846..5271321hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023286
Supporting Variants
Samples
Known GenesRABEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620107
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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