A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901805



Internal ID22676958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167911293..167911865hg38UCSC Ensembl
chr3:167629081..167629653hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423470
Samples
Known GenesLOC646168
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901805
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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