A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940977



Internal ID21361046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130785608..130785608hg38UCSC Ensembl
chr10:132583872..132583872hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191301
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940977
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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