A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431984



Internal ID21393986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33544864..33553863hg38UCSC Ensembl
chr13:34119001..34128000hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751232
SamplesBTQ055
Known GenesSTARD13
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431984
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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