A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv616e199



Internal ID20123918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4974059..4976265hg38UCSC Ensembl
chr19:4974070..4976276hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382207
hg192207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2662008, esv2667758
SamplesNA18605, NA18550, NA18564, NA18613, NA18940, HG00590, NA18565, NA18944
Known GenesKDM4B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv616e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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