A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732741



Internal ID20508666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132018178..132020079hg38UCSC Ensembl
chr7:131702937..131704838hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271859
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732741
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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