A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208092



Internal ID22356387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83187290..83187386hg38UCSC Ensembl
chr15:83856042..83856138hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377979
SamplesNA19240
Known GenesHDGFRP3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208092
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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