A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442917



Internal ID221328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150605459..150605548hg38UCSC Ensembl
chr3:150323246..150323335hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940538
Samples
Known GenesSELT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442917
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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