A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628982



Internal ID7015804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28937555..28945816hg38UCSC Ensembl
Innerchr12:28937555..28945816hg38UCSC Ensembl
Outerchr12:28937503..28945990hg38UCSC Ensembl
chr12:29090488..29098749hg19UCSC Ensembl
Innerchr12:29090488..29098749hg19UCSC Ensembl
Outerchr12:29090436..29098923hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg388262
hg198262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14422674
SamplesHG03012
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628982
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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