A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3249562



Internal ID22377308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93734789..93734877hg38UCSC Ensembl
chr15:94278018..94278106hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14445800
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsInsertion variant involving MER satellite DNA
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3249562
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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