A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192590



Internal ID22343150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77583922..77584114hg38UCSC Ensembl
chr11:77294967..77295159hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390258
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192590
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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