A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6239846



Internal ID22044456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141166480..141166480hg38UCSC Ensembl
chr7:140866280..140866280hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17839336
Samples
Known GenesTMEM178B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6239846
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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