A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202739



Internal ID22351858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117097601..117097652hg38UCSC Ensembl
chr8:118109840..118109891hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14460685
SamplesHG00733
Known GenesSLC30A8
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202739
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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