A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746832



Internal ID21385624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129424722..129444721hg38UCSC Ensembl
chr9:132187001..132207000hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3820000
hg1920000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435638
Supporting Variants
SamplesBTQ055
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746832
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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