A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486133



Internal ID263507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112016279..112080522hg38UCSC Ensembl
chr7:111656334..111720577hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3864244
hg1964244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735726
Samples
Known GenesDOCK4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486133
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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