A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676132



Internal ID9595551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:11014619..11069778hg38UCSC Ensembl
Outerchr12:11014581..11069818hg38UCSC Ensembl
Innerchr12:11167218..11222377hg19UCSC Ensembl
Outerchr12:11167180..11222417hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3855238
hg1955238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv265e199
Supporting Variantsessv6557921, essv6058173
SamplesNA20506, HG00407
Known GenesPRH1-PRR4, TAS2R19, TAS2R31, TAS2R46
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676132
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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