A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732112



Internal ID20508035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194381990..194382092hg38UCSC Ensembl
chr3:194102719..194102821hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732112
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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