A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764869



Internal ID20540729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84961105..84961105hg38UCSC Ensembl
chr7:84590421..84590421hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764869
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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