A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021553



Internal ID21930896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42812115..42812292hg38UCSC Ensembl
chr17:40964133..40964310hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636294
Samples
Known GenesBECN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021553
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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