A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075480



Internal ID21984713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115411489..115411489hg38UCSC Ensembl
chr7:115051543..115051543hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg381898
hg191898
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568094
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075480
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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