A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733537



Internal ID20509467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35628578..35628637hg38UCSC Ensembl
chr1:36094179..36094238hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285533
Samples
Known GenesPSMB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733537
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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