A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734051



Internal ID20509984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13031453..13031521hg38UCSC Ensembl
chr3:13072953..13073021hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261204
Samples
Known GenesIQSEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734051
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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