A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768051



Internal ID20543911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125227981..125227981hg38UCSC Ensembl
chr10:126916550..126916550hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768051
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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