A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905721



Internal ID22680912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9597629..9602125hg38UCSC Ensembl
chr3:9639313..9643809hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg384497
hg194497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905721
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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