A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433861



Internal ID21395863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108553148..108554041hg38UCSC Ensembl
chr3:108271995..108272888hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38894
hg19894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753871
SamplesMDQ025
Known GenesKIAA1524
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433861
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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