A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1163e214



Internal ID22757057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3331357..3336086hg38UCSC Ensembl
chr6:3331591..3336320hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384730
hg194730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3607928, esv3607927
SamplesNA19076, HG00475, NA18637
Known GenesSLC22A23
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1163e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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