A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14386909



Internal ID22310685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47896327..47896433hg38UCSC Ensembl
chr10:47061089..47061195hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192378
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)nssv14386909
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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