A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628001



Internal ID6668145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126290636..126292851hg38UCSC Ensembl
Innerchr11:126290641..126292846hg38UCSC Ensembl
Outerchr11:126290631..126292856hg38UCSC Ensembl
chr11:126160531..126162746hg19UCSC Ensembl
Innerchr11:126160536..126162741hg19UCSC Ensembl
Outerchr11:126160526..126162751hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382216
hg192216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14302925, essv14302926, essv14302924, essv14302923
SamplesNA18542, HG02020, NA18593, NA19078
Known GenesTIRAP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628001
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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