A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669258



Internal ID9935363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159111834..159111914hg38UCSC Ensembl
chr6:159532866..159532946hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5468771, essv5876020, essv5516425, essv6186065, essv6177712, essv6014321, essv6282210, essv5396480, essv5684816, essv6546109, essv5515834, essv6117472, essv6441860, essv5932291
SamplesHG01066, HG00251, HG00702, HG00689, HG00137, HG00275, NA18534, HG00619, HG00284, HG00250, HG00704, NA18576, HG00285, NA18517
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669258
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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