A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749066



Internal ID20525095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70133099..70133156hg38UCSC Ensembl
chr10:71892855..71892912hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268194
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749066
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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