A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950232



Internal ID21370301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70126760..70126760hg38UCSC Ensembl
chr11:69972866..69972866hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191483
SamplesHG002
Known GenesANO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950232
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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