A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903412



Internal ID22678579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:80573087..80639967hg38UCSC Ensembl
chr3:80622237..80689118hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3866881
hg1966882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903412
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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