A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626012



Internal ID7012846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38587688..38590362hg38UCSC Ensembl
Innerchr11:38587738..38590312hg38UCSC Ensembl
Outerchr11:38587604..38590446hg38UCSC Ensembl
chr11:38609238..38611912hg19UCSC Ensembl
Innerchr11:38609288..38611862hg19UCSC Ensembl
Outerchr11:38609154..38611996hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382675
hg192675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14095209
SamplesHG02146
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626012
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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