A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032286



Internal ID21941629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21047754..21053468hg38UCSC Ensembl
chr17:20951067..20956781hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg385715
hg195715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032286
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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