A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739386



Internal ID20515359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137448556..137448629hg38UCSC Ensembl
chr7:137133302..137133375hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294024
Samples
Known GenesDGKI
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739386
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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