A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203894



Internal ID22352836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118556625..118556765hg38UCSC Ensembl
chr10:120316137..120316277hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14414274
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203894
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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