A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6409283



Internal ID9896920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75348489..75353834hg38UCSC Ensembl
chr9:77963405..77968750hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385346
hg195346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657752
Supporting Variants
SamplesNA20785
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6409283
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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