A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892839



Internal ID22667895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141377949..141378174hg38UCSC Ensembl
chr3:141096791..141097016hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391459
Samples
Known GenesZBTB38
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892839
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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