A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027603



Internal ID21936946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50656575..50662905hg38UCSC Ensembl
chr17:48733936..48740266hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg386331
hg196331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629772
Samples
Known GenesABCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027603
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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