A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198316



Internal ID22348059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86469249..86469306hg38UCSC Ensembl
chr10:88229006..88229063hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1004n152
Supporting Variantsnssv14387252
SamplesNA19240
Known GenesWAPAL
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198316
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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