A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748746



Internal ID20524773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50487670..50487740hg38UCSC Ensembl
chr19:50990927..50990997hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284128
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748746
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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