A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625314



Internal ID7012149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8427961..8428521hg38UCSC Ensembl
Innerchr11:8427991..8428492hg38UCSC Ensembl
Outerchr11:8427932..8428551hg38UCSC Ensembl
chr11:8449508..8450068hg19UCSC Ensembl
Innerchr11:8449538..8450039hg19UCSC Ensembl
Outerchr11:8449479..8450098hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14018287, essv14018286
SamplesNA20355, NA19360
Known GenesSTK33
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625314
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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