A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667451



Internal ID9933556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18404025..18404916hg38UCSC Ensembl
Outerchr19:18403868..18405069hg38UCSC Ensembl
Innerchr19:18514835..18515726hg19UCSC Ensembl
Outerchr19:18514678..18515879hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6258120, essv6573375
SamplesNA18907, NA19093
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667451
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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