A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628556



Internal ID6668699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10995613..11052888hg38UCSC Ensembl
Innerchr12:10995649..11052853hg38UCSC Ensembl
Outerchr12:10995578..11052924hg38UCSC Ensembl
chr12:11148212..11205487hg19UCSC Ensembl
Innerchr12:11148248..11205452hg19UCSC Ensembl
Outerchr12:11148177..11205523hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3857276
hg1957276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14378634
SamplesNA19681
Known GenesPRH1-PRR4, TAS2R19, TAS2R20, TAS2R31
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628556
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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