A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227527



Internal ID22369993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61459271..61465750hg38UCSC Ensembl
chr9:40478940..40485345hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg386480
hg196406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9570n152
Supporting Variantsnssv14439737
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227527
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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