A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294024



Internal ID20503242
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 StatusS
Merged Variantsnsv4739386
Supporting Variants
Samples
Known GenesDGKI
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294024
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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