A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5863587



Internal ID9159572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25258418..25352564hg38UCSC Ensembl
Outerchr9:25258384..25352599hg38UCSC Ensembl
Innerchr9:25258416..25352562hg19UCSC Ensembl
Outerchr9:25258382..25352597hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3894216
hg1994216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674023
Supporting Variants
SamplesHG01354
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5863587
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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