A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196666



Internal ID22346641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91554688..91554803hg38UCSC Ensembl
chr10:93314445..93314560hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14439287
SamplesHG00733
Known GenesLOC100188947
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196666
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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