A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459383



Internal ID22211938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11185171..11185429hg38UCSC Ensembl
chr6:11185404..11185662hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3174757
Supporting Variants
SamplesHG00733
Known GenesNEDD9
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14459383
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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