A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435670



Internal ID21397672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134595155..134600154hg38UCSC Ensembl
chr9:137487001..137492000hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv872n172
Supporting Variantsnssv15747870
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435670
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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