A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626577



Internal ID6666727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61257434..61267693hg38UCSC Ensembl
Innerchr11:61257434..61267693hg38UCSC Ensembl
Outerchr11:61257329..61267734hg38UCSC Ensembl
chr11:61024906..61035165hg19UCSC Ensembl
Innerchr11:61024906..61035165hg19UCSC Ensembl
Outerchr11:61024801..61035206hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3810260
hg1910260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14176370
SamplesNA12489
Known GenesVWCE
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626577
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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