A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456305



Internal ID234375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140739047..140739149hg38UCSC Ensembl
chr4:141660201..141660303hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16955389
Samples
Known GenesTBC1D9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456305
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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