A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674132



Internal ID9940237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11158260..11159399hg38UCSC Ensembl
Outerchr19:11158223..11159449hg38UCSC Ensembl
Innerchr19:11268936..11270075hg19UCSC Ensembl
Outerchr19:11268899..11270125hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381227
hg191227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6479994
SamplesHG00690
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674132
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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