A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896561



Internal ID22671655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40712255..40712936hg38UCSC Ensembl
chr3:40753746..40754427hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896561
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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