A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433888



Internal ID21395890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13009501..13028500hg38UCSC Ensembl
chr3:13051001..13070000hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3819000
hg1919000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv506n172
Supporting Variantsnssv15749407
SamplesSMI034
Known GenesIQSEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433888
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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