A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761052



Internal ID20536912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143808340..143808340hg38UCSC Ensembl
chr8:144890510..144890510hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285215
Samples
Known GenesSCRIB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761052
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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