A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934996



Internal ID21355065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76718908..76718908hg38UCSC Ensembl
chr11:76429952..76429952hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190928
SamplesHG002
Known GenesGUCY2EP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934996
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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