A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6118226



Internal ID9095629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:11016540..11072168hg38UCSC Ensembl
Outerchr12:11016506..11072203hg38UCSC Ensembl
Innerchr12:11169139..11224767hg19UCSC Ensembl
Outerchr12:11169105..11224802hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3855698
hg1955698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674625
Supporting Variants
SamplesHG00332
Known GenesPRH1-PRR4, TAS2R19, TAS2R31, TAS2R46
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6118226
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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