A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025709



Internal ID21935052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68634372..68634441hg38UCSC Ensembl
chr17:66630513..66630582hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025709
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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