A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993687



Internal ID63248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12415395..12453284hg38UCSC Ensembl
chr7:12455021..12492910hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3837890
hg1937890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462229
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993687
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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