A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671087



Internal ID9937192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4036334..4036656hg38UCSC Ensembl
Outerchr19:4036297..4036706hg38UCSC Ensembl
Innerchr19:4036332..4036654hg19UCSC Ensembl
Outerchr19:4036295..4036704hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5740915, essv6136272, essv5744876, essv6528934, essv5556345, essv5628213, essv5848461, essv5713885, essv6093327, essv5652054, essv6013780, essv5776730, essv5831424, essv5712914, essv5836767, essv6316317, essv5750746, essv6452792, essv5528605, essv5708263, essv5419243, essv5415561, essv5412890
SamplesNA18502, NA19700, NA18861, NA18507, NA18917, NA19393, NA19190, NA18916, NA19657, NA19707, NA18933, NA20344, NA18499, NA18523, HG00285, NA19321, NA19147, NA19360, NA18501, NA19223, NA19102, NA19129, NA19316
Known GenesPIAS4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671087
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer