A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210297



Internal ID22358239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72559203..72559265hg38UCSC Ensembl
chr9:75174119..75174181hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14459329
SamplesHG00733
Known GenesTMC1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210297
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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