A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936645



Internal ID21356714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125824766..125824766hg38UCSC Ensembl
chr10:127513335..127513335hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191752
SamplesHG002
Known GenesBCCIP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936645
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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