A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625070



Internal ID6665223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:553728..559392hg38UCSC Ensembl
Innerchr11:553728..559392hg38UCSC Ensembl
Outerchr11:553633..559496hg38UCSC Ensembl
chr11:553728..559392hg19UCSC Ensembl
Innerchr11:553728..559392hg19UCSC Ensembl
Outerchr11:553633..559496hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg385665
hg195665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13989824
SamplesHG01865
Known GenesC11orf35, LRRC56
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625070
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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