A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628120



Internal ID6668264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132209430..132211574hg38UCSC Ensembl
Innerchr11:132209456..132211549hg38UCSC Ensembl
Outerchr11:132209405..132211600hg38UCSC Ensembl
chr11:132079324..132081468hg19UCSC Ensembl
Innerchr11:132079350..132081443hg19UCSC Ensembl
Outerchr11:132079299..132081494hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382145
hg192145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14317585
SamplesNA12717
Known GenesNTM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628120
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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