A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028061



Internal ID21937404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76107350..76115851hg38UCSC Ensembl
chr17:74103431..74111932hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg388502
hg198502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028061
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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