A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv208e214



Internal ID22756102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72141339..72179940hg38UCSC Ensembl
chr11:71852383..71890984hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3838602
hg1938602
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3626793, esv3626792
SamplesHG00142, HG02634, NA19917, HG00266, HG03898
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv208e214
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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