A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757037



Internal ID20532897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78226793..78226793hg38UCSC Ensembl
chr15:78519135..78519135hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295758
Samples
Known GenesACSBG1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757037
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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