A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761277



Internal ID20537137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89998342..89998342hg38UCSC Ensembl
chr10:91758099..91758099hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761277
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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