A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060846



Internal ID21970079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19098560..19098560hg38UCSC Ensembl
chr7:19138183..19138183hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568692
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060846
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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