A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204297



Internal ID22353170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137720127..137724127hg38UCSC Ensembl
chr9:140614579..140618579hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg384001
hg194001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14378163, nssv14372666
SamplesNA19240
Known GenesEHMT1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204297
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer