A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899137



Internal ID22674263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196124499..196129845hg38UCSC Ensembl
chr3:195851370..195856716hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg385347
hg195347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899137
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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