A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14095209



Internal ID2433894
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626012
Supporting Variants
SamplesHG02146
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14095209
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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