A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892611



Internal ID22667664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156701413..156701591hg38UCSC Ensembl
chr3:156419202..156419380hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410389
Samples
Known GenesTIPARP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892611
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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