A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199178



Internal ID22348801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134992254..134992318hg38UCSC Ensembl
chr9:137884100..137884164hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9808n152
Supporting Variantsnssv14464173
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199178
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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