A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658409



Internal ID9577828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42467824..42468751hg38UCSC Ensembl
Outerchr19:42467787..42468801hg38UCSC Ensembl
Innerchr19:42971976..42972903hg19UCSC Ensembl
Outerchr19:42971939..42972953hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381015
hg191015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5537162, essv6397153
SamplesHG00309, NA07037
Known GenesLIPE-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658409
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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