A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14390258



Internal ID22304972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77583922..77584114hg38UCSC Ensembl
chr11:77294967..77295159hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192590
Supporting Variants
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)nssv14390258
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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