A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060992



Internal ID21970225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20278039..20278039hg38UCSC Ensembl
chr7:20317662..20317662hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060992
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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