A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1111e214



Internal ID22757005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84713401..84820752hg38UCSC Ensembl
chr5:84009219..84116570hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38107352
hg19107352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3605657, esv3605656
SamplesHG03717, HG03762, HG03786, NA20875, HG03238, HG03012, HG04023, NA20847, HG02778, HG03989
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1111e214
Frequency
Sample Size2504
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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