A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284996



Internal ID20494214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134665251..134665675hg38UCSC Ensembl
chr7:134350003..134350427hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745824
Supporting Variants
Samples
Known GenesBPGM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284996
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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