A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481718



Internal ID259188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95048923..95049053hg38UCSC Ensembl
chr7:94678235..94678365hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735719
Samples
Known GenesPPP1R9A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481718
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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