A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934931



Internal ID24018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61898800..61976879hg38UCSC Ensembl
chr3:61884474..61962553hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3878080
hg1978080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451148
Supporting Variants
Samples
Known GenesPTPRG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934931
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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