A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690059



Internal ID113725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95714413..95714527hg38UCSC Ensembl
chr12:96108191..96108305hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510523
Supporting Variants
Samples
Known GenesNTN4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690059
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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