A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744492



Internal ID20520491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192828601..192828661hg38UCSC Ensembl
chr3:192546390..192546450hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276362
Samples
Known GenesMB21D2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744492
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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