A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14404620



Internal ID22325213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49861026..49861078hg38UCSC Ensembl
chr15:50153223..50153275hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210238
Supporting Variants
SamplesNA19240
Known GenesATP8B4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14404620
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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