A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995896



Internal ID64702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51728268..51775987hg38UCSC Ensembl
chr7:51795964..51843683hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3847720
hg1947720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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