A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192014



Internal ID22342651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137715108..137717533hg38UCSC Ensembl
chr9:140609560..140611985hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382426
hg192426
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14412563
SamplesHG00514
Known GenesEHMT1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192014
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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