A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197413



Internal ID22347300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74050712..74051278hg38UCSC Ensembl
chr11:73761757..73762323hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377733
SamplesNA19240
Known GenesC2CD3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197413
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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