A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15805292



Internal ID3442429
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641790
Supporting Variants
SamplesHG03073
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15805292
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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