A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012184



Internal ID21921527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141411006..141411155hg38UCSC Ensembl
chr7:141110806..141110955hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569748
Samples
Known GenesTMEM178B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012184
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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