A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752960



Internal ID20528820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122644023..122644023hg38UCSC Ensembl
chr10:124403539..124403539hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752960
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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