A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207397



Internal ID22355789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35045651..35045720hg38UCSC Ensembl
chr19:35536555..35536624hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14432258
SamplesHG00514
Known GenesHPN
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207397
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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