A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743076



Internal ID20519062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131839560..131839871hg38UCSC Ensembl
chr7:131524319..131524630hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290778
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743076
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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