A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738514



Internal ID20514484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36764325..36765178hg38UCSC Ensembl
chr9:36764322..36765175hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273189
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738514
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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