A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892095



Internal ID22667140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129516132..129516229hg38UCSC Ensembl
chr3:129234975..129235072hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394660
Samples
Known GenesIFT122
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892095
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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