A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14399869



Internal ID22299263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134441121..134442921hg38UCSC Ensembl
chr5:133776812..133778612hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3175829
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)nssv14399869
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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