A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626843



Internal ID7013673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74537989..74547287hg38UCSC Ensembl
Innerchr11:74537989..74547287hg38UCSC Ensembl
Outerchr11:74537814..74547529hg38UCSC Ensembl
chr11:74249034..74258332hg19UCSC Ensembl
Innerchr11:74249034..74258332hg19UCSC Ensembl
Outerchr11:74248859..74258574hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg389299
hg199299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14213958
SamplesHG01137
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626843
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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