A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191402



Internal ID22342113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119646882..119647038hg38UCSC Ensembl
chr11:119517592..119517748hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14418732
SamplesHG00514
Known GenesPVRL1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191402
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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