A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628091



Internal ID7014916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130787394..130790339hg38UCSC Ensembl
Innerchr11:130787394..130790339hg38UCSC Ensembl
Outerchr11:130787329..130790399hg38UCSC Ensembl
chr11:130657289..130660234hg19UCSC Ensembl
Innerchr11:130657289..130660234hg19UCSC Ensembl
Outerchr11:130657224..130660294hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382946
hg192946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14312662
SamplesHG03730
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628091
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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