A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1114e214



Internal ID22757008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97222067..97320665hg38UCSC Ensembl
chr5:96557771..96656369hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3898599
hg1998599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3605876, esv3605875
SamplesHG00584, NA20289
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1114e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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