A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991732



Internal ID61915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1107979..1108351hg38UCSC Ensembl
chr7:1147615..1147987hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463058
Supporting Variants
Samples
Known GenesC7orf50
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991732
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.047158


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