A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv644e199



Internal ID22758417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41186238..41191937hg38UCSC Ensembl
chr19:41692143..41697842hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2664943, esv2669501
SamplesNA19394, NA19443, NA19107, NA19373, NA19379, NA19197, NA19313, NA19404, NA19172, NA19347, NA18933, NA19391, NA19455, HG00740, NA19114, NA19318, NA19436, HG01148, NA19440, NA19331, NA19334, NA19467, NA19438, NA19468, NA19430, NA19429, NA19346, NA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv644e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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