A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199069



Internal ID22348708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127503339..127503592hg38UCSC Ensembl
chr9:130265618..130265871hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14439894
SamplesHG00733
Known GenesLRSAM1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199069
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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