A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748393



Internal ID20524418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19871752..19871900hg38UCSC Ensembl
chr1:20198245..20198393hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748393
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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