A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086976



Internal ID21996209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114787682..114787682hg38UCSC Ensembl
chr10:116547441..116547441hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086976
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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