A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761073



Internal ID20536933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72111383..72111383hg38UCSC Ensembl
chr8:73023618..73023618hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg381673
hg191673
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761073
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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