A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761055



Internal ID20536915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22801069..22801069hg38UCSC Ensembl
chr7:22840688..22840688hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761055
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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