A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657925



Internal ID9924030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136735071..136751130hg38UCSC Ensembl
chr9:139629523..139645582hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3816060
hg1916060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5741413
SamplesHG00319
Known GenesLCN10, LCN6, LOC100128593, MIR6722
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657925
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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