A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993177



Internal ID62905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20573487..20575660hg38UCSC Ensembl
chr7:20613110..20615283hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg382174
hg192174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468702
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993177
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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