A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737501



Internal ID20513462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143265428..143265506hg38UCSC Ensembl
chr8:144347598..144347676hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272889
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737501
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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