A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195224



Internal ID22345436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:310837..318932hg38UCSC Ensembl
chr11:310837..318932hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388096
hg198096
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14440293
SamplesHG00733
Known GenesIFITM1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195224
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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