A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv668e214



Internal ID22756562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50752126..50763917hg38UCSC Ensembl
chr19:51255383..51267174hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3811792
hg1911792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3644652, esv3644650
SamplesNA18565, HG02433, HG02155, HG00598, HG02807, HG03695, HG01866, HG01933, HG04061
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv668e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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