A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16999099



Internal ID66965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93163853..93167577hg38UCSC Ensembl
chr7:92793166..92796890hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg383725
hg193725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16999099
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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