A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731211



Internal ID20507129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37958903..37959219hg38UCSC Ensembl
chr7:37998505..37998821hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731211
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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