A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627565



Internal ID7014393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103883217..103885046hg38UCSC Ensembl
Innerchr11:103883217..103885046hg38UCSC Ensembl
Outerchr11:103883044..103885215hg38UCSC Ensembl
chr11:103753945..103755774hg19UCSC Ensembl
Innerchr11:103753945..103755774hg19UCSC Ensembl
Outerchr11:103753772..103755943hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381830
hg191830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14258228
SamplesHG01811
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627565
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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