A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14414389



Internal ID22149796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60982123..60982174hg38UCSC Ensembl
chr11:60749595..60749646hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198386
Supporting Variants
SamplesHG00514
Known GenesCD6
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14414389
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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