A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736860



Internal ID20512813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124267724..124267992hg38UCSC Ensembl
chr8:125279965..125280233hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295608
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736860
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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