A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5527439



Internal ID8881419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27740586..27744055hg38UCSC Ensembl
Outerchr9:27740429..27744208hg38UCSC Ensembl
Innerchr9:27740584..27744053hg19UCSC Ensembl
Outerchr9:27740427..27744206hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg383780
hg193780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678973
Supporting Variants
SamplesHG00331
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5527439
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