A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738741



Internal ID20514712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138392480..138392658hg38UCSC Ensembl
chr7:138077225..138077403hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738741
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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