A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040260



Internal ID21949603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79709786..79709874hg38UCSC Ensembl
chr17:77683594..77683682hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629219
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040260
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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