A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3409932



Internal ID15256892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78134138..78134154hg38UCSC Ensembl
Innerchr11:78134145..78134147hg38UCSC Ensembl
Outerchr11:78134131..78134161hg38UCSC Ensembl
chr11:77845184..77845200hg19UCSC Ensembl
Innerchr11:77845191..77845193hg19UCSC Ensembl
Outerchr11:77845177..77845207hg19UCSC Ensembl
chr11:77522832..77522848hg18UCSC Ensembl
Innerchr11:77522839..77522841hg18UCSC Ensembl
Outerchr11:77522825..77522855hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865497
SamplesNA12005
Known GenesALG8
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3409932
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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