A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5825676



Internal ID8803079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112434804..112437710hg38UCSC Ensembl
chr9:115197084..115199990hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382907
hg192907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678312
Supporting Variants
SamplesNA19247
Known GenesHSDL2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5825676
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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