A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627243



Internal ID7014073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91229537..91313990hg38UCSC Ensembl
Innerchr11:91229593..91313934hg38UCSC Ensembl
Outerchr11:91229481..91314046hg38UCSC Ensembl
chr11:90962705..91047157hg19UCSC Ensembl
Innerchr11:90962761..91047101hg19UCSC Ensembl
Outerchr11:90962649..91047213hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3884454
hg1984453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14233022, essv14233023
SamplesHG02386, NA18605
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627243
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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