A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019415



Internal ID21928758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80933985..80958123hg38UCSC Ensembl
chr7:80563301..80587439hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3824139
hg1924139
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572876
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019415
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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