A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756384



Internal ID20532244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130734053..130734053hg38UCSC Ensembl
chr7:130418880..130418880hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756384
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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