A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669728



Internal ID9935833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:100116305..100118368hg38UCSC Ensembl
Outerchr9:100116268..100118418hg38UCSC Ensembl
Innerchr9:102878587..102880650hg19UCSC Ensembl
Outerchr9:102878550..102880700hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382151
hg192151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6483724
SamplesHG00182
Known GenesINVS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669728
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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