A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5741413



Internal ID8863248
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 Flag1
Merged StatusS
Merged Variantsesv2657925
Supporting Variants
SamplesHG00319
Known GenesLCN10, LCN6, LOC100128593, MIR6722
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5741413
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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