A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439255



Internal ID217795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159282580..159282684hg38UCSC Ensembl
chr3:159000369..159000473hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941633
Samples
Known GenesIQCJ-SCHIP1, MIR3919, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439255
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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