A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16996361



Internal ID65026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52853373..52919295hg38UCSC Ensembl
chr7:52921066..52986988hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3865923
hg1965923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487459
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16996361
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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