A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563333



Internal ID336268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141081968..141086228hg38UCSC Ensembl
chr7:140781768..140786028hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg384261
hg194261
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004681
Samples
Known GenesTMEM178B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563333
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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