A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752891



Internal ID20528751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72347205..72347205hg38UCSC Ensembl
chr15:72639546..72639546hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288929
Samples
Known GenesHEXA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752891
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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