A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14404602



Internal ID22325777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42350282..42350808hg38UCSC Ensembl
chr15:42642480..42643006hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197397
Supporting Variants
SamplesNA19240
Known GenesGANC
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14404602
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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