A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1113e214



Internal ID18981288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95963962..96119963hg38UCSC Ensembl
chr5:95299666..95455667hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38156002
hg19156002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3605844, esv3605842
SamplesNA18582, NA19434, NA19468
Known GenesMIR583
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1113e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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