A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14394122



Internal ID22285413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68687743..68687834hg38UCSC Ensembl
chr2:68914875..68914966hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3184043
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)nssv14394122
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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