A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477902



Internal ID255468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157562985..157563336hg38UCSC Ensembl
chr7:157355678..157356029hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17007841
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477902
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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