A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931797



Internal ID21351866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89998341..89998341hg38UCSC Ensembl
chr10:91758098..91758098hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192132
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931797
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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