A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098189



Internal ID22007422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126121408..126121408hg38UCSC Ensembl
chr10:127809977..127809977hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590842
Samples
Known GenesADAM12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098189
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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