A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190529



Internal ID22341382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92571521..92571600hg38UCSC Ensembl
chr15:93114751..93114830hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14417706, nssv14374874
SamplesNA19240, HG00514
Known GenesLINC00930
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190529
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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