A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625797



Internal ID7012631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29392719..29398824hg38UCSC Ensembl
Innerchr11:29392754..29398790hg38UCSC Ensembl
Outerchr11:29392685..29398859hg38UCSC Ensembl
chr11:29414266..29420371hg19UCSC Ensembl
Innerchr11:29414301..29420337hg19UCSC Ensembl
Outerchr11:29414232..29420406hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg386106
hg196106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14076662, essv14076663, essv14076659, essv14076660, essv14076661
SamplesHG02734, NA12748, HG03756, HG03743, HG03849
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625797
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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