A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510793



Internal ID287400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:128488520..128499148hg38UCSC Ensembl
chr12:128973065..128983693hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3810629
hg1910629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17685322
Samples
Known GenesTMEM132C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510793
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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