A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660622



Internal ID9926727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18759215..18761577hg38UCSC Ensembl
Outerchr7:18759178..18761627hg38UCSC Ensembl
Innerchr7:18798838..18801200hg19UCSC Ensembl
Outerchr7:18798801..18801250hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg382450
hg192450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5642895
SamplesNA19012
Known GenesHDAC9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660622
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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