A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019876



Internal ID21929219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107847475..107847534hg38UCSC Ensembl
chr7:107487920..107487979hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019876
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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