A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732893



Internal ID20508819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160783880..160784500hg38UCSC Ensembl
chr3:160501668..160502288hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295058
Samples
Known GenesPPM1L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732893
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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