A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263474



Internal ID20472692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148810713..148810777hg38UCSC Ensembl
chr7:148507805..148507869hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742079
Supporting Variants
Samples
Known GenesEZH2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263474
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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