A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627730



Internal ID6667877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111289595..111291946hg38UCSC Ensembl
Innerchr11:111289595..111291946hg38UCSC Ensembl
Outerchr11:111289343..111292287hg38UCSC Ensembl
chr11:111160320..111162671hg19UCSC Ensembl
Innerchr11:111160320..111162671hg19UCSC Ensembl
Outerchr11:111160068..111163012hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg382352
hg192352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14286885, essv14286887, essv14286886
SamplesHG02131, HG01872, NA18623
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627730
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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