A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937060



Internal ID21357129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62928909..62928909hg38UCSC Ensembl
chr10:64688669..64688669hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191652
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937060
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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