A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746400



Internal ID20522413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128118510..128118639hg38UCSC Ensembl
chr8:129130756..129130885hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266552
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746400
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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