A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083973



Internal ID21993206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119684572..119684572hg38UCSC Ensembl
chr10:121444084..121444084hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083973
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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