A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17007837



Internal ID72850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157553844..157554470hg38UCSC Ensembl
chr7:157346538..157347164hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142709
Supporting Variants
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17007837
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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