A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17003696



Internal ID70089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135495869..135497182hg38UCSC Ensembl
chr7:135180617..135181930hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381314
hg191314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484649
Supporting Variants
Samples
Known GenesCNOT4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17003696
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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