A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641790



Internal ID7028561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11177300..11190342hg38UCSC Ensembl
Innerchr18:11177300..11190342hg38UCSC Ensembl
Outerchr18:11177256..11190558hg38UCSC Ensembl
chr18:11177299..11190341hg19UCSC Ensembl
Innerchr18:11177299..11190341hg19UCSC Ensembl
Outerchr18:11177255..11190557hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3813043
hg1913043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv601e214
Supporting Variantsessv15805292
SamplesHG03073
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641790
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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