A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627398



Internal ID7014227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97101748..97177736hg38UCSC Ensembl
Innerchr11:97101769..97177715hg38UCSC Ensembl
Outerchr11:97101727..97177757hg38UCSC Ensembl
chr11:96972748..97048736hg19UCSC Ensembl
Innerchr11:96972769..97048715hg19UCSC Ensembl
Outerchr11:96972727..97048757hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3875989
hg1975989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14245467, essv14245463, essv14245464, essv14245462, essv14245466, essv14245461, essv14245465
SamplesHG02922, HG03159, HG02508, HG03123, NA18912, HG03437, HG02546
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627398
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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