A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625856



Internal ID7012690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32324602..32328822hg38UCSC Ensembl
Innerchr11:32324606..32328819hg38UCSC Ensembl
Outerchr11:32324599..32328826hg38UCSC Ensembl
chr11:32346148..32350368hg19UCSC Ensembl
Innerchr11:32346152..32350365hg19UCSC Ensembl
Outerchr11:32346145..32350372hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384221
hg194221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14080052
SamplesNA11930
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625856
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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