A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14414918



Internal ID22150386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11500657..11501037hg38UCSC Ensembl
chr10:11542656..11543036hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199603
Supporting Variants
SamplesHG00514
Known GenesUSP6NL
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14414918
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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