A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5861341



Internal ID9434949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1950217..1951623hg38UCSC Ensembl
Outerchr19:1949596..1952093hg38UCSC Ensembl
Innerchr19:1950216..1951622hg19UCSC Ensembl
Outerchr19:1949595..1952092hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382498
hg192498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661504
Supporting Variants
SamplesNA18635
Known GenesCSNK1G2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5861341
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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