A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904245



Internal ID22679421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196973607..196973722hg38UCSC Ensembl
chr3:196700478..196700593hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424134
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904245
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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