A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893412



Internal ID22668472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:110248351..110248649hg38UCSC Ensembl
chr3:109967198..109967496hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893412
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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