A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026828



Internal ID21936171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19825598..19825878hg38UCSC Ensembl
chr17:19728911..19729191hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630848
Samples
Known GenesULK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026828
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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