A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434609



Internal ID213279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170077528..170078953hg38UCSC Ensembl
chr3:169795316..169796741hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381426
hg191426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942472
Samples
Known GenesGPR160
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434609
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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