A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489240



Internal ID266529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149105849..149107457hg38UCSC Ensembl
chr7:148802941..148804549hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg381609
hg191609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004780
Samples
Known GenesZNF425
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489240
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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