A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016226



Internal ID21925569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97939141..97939325hg38UCSC Ensembl
chr7:97568453..97568637hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016226
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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