A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937697



Internal ID21357766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62143052..62143052hg38UCSC Ensembl
chr11:61910524..61910524hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191445
SamplesHG002
Known GenesINCENP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937697
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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