A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740155



Internal ID20516130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93116036..93116105hg38UCSC Ensembl
chr10:94875793..94875862hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296195
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740155
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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