A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198917



Internal ID22348582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51345810..51345866hg38UCSC Ensembl
chr19:51849064..51849120hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14420959
SamplesHG00514
Known GenesETFB
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198917
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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