A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435772



Internal ID21397774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79934086..79935085hg38UCSC Ensembl
chr9:82549001..82550000hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747711
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435772
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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