A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14443884



Internal ID22227486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134138367..134138440hg38UCSC Ensembl
chr11:134008262..134008335hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192928
Supporting Variants
SamplesHG00733
Known GenesJAM3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14443884
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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