A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5426309



Internal ID9803380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105610091..105611054hg38UCSC Ensembl
Outerchr9:105609934..105611207hg38UCSC Ensembl
Innerchr9:108372372..108373335hg19UCSC Ensembl
Outerchr9:108372215..108373488hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381274
hg191274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678852
Supporting Variants
SamplesNA19900
Known GenesFKTN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5426309
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