A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993435



Internal ID63078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12951505..12969298hg38UCSC Ensembl
chr7:12991130..13008923hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3817794
hg1917794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472938
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993435
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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