A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733106



Internal ID20509033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55728507..55729007hg38UCSC Ensembl
chr1:56194180..56194680hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733106
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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