A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936680



Internal ID21356749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47557553..47557553hg38UCSC Ensembl
chr11:47579105..47579105hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192697
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936680
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer