A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947117



Internal ID22722619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57061436..57061742hg38UCSC Ensembl
chr12:57455219..57455525hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368930
Samples
Known GenesTMEM194A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947117
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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