A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628665



Internal ID7015489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15272300..15295466hg38UCSC Ensembl
Innerchr12:15272311..15295456hg38UCSC Ensembl
Outerchr12:15272290..15295477hg38UCSC Ensembl
chr12:15425234..15448400hg19UCSC Ensembl
Innerchr12:15425245..15448390hg19UCSC Ensembl
Outerchr12:15425224..15448411hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3823167
hg1923167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14395067, essv14395066
SamplesNA20775, NA20778
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628665
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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