A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677201



Internal ID9943306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4662933..4663557hg38UCSC Ensembl
Outerchr19:4662896..4663607hg38UCSC Ensembl
Innerchr19:4662945..4663569hg19UCSC Ensembl
Outerchr19:4662908..4663619hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5586352, essv5628441, essv5988853, essv5589502, essv5887589
SamplesHG01389, HG01051, NA19088, NA18544, NA18637
Known GenesC19orf10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677201
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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