A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3544134



Internal ID22413176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32331299..32331299hg38UCSC Ensembl
chr11:32352845..32352845hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3816934
hg1916934
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14416295
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3544134
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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