A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018073



Internal ID21927416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108954980..109003900hg38UCSC Ensembl
chr7:108595037..108643957hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3848921
hg1948921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567970
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018073
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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