A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736689



Internal ID20512641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100419481..100419535hg38UCSC Ensembl
chr10:102179238..102179292hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736689
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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