A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767448



Internal ID20543308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90685034..90685034hg38UCSC Ensembl
chr8:91697262..91697262hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767448
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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