A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1112e214



Internal ID20122535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95706463..95713774hg38UCSC Ensembl
chr5:95042167..95049478hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg387312
hg197312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3605837, esv3605836
SamplesHG01815, NA19717, HG04054, HG02408, HG02019, HG01804, HG02462
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1112e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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