A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259579



Internal ID20468797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46326826..46327146hg38UCSC Ensembl
chr7:46366424..46366744hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742799
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259579
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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