A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435635



Internal ID21397637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129424722..129435721hg38UCSC Ensembl
chr9:132187001..132198000hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3811000
hg1911000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749453
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435635
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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