A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1297e214



Internal ID22757191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66465118..66477819hg38UCSC Ensembl
chr7:65930105..65942806hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3812702
hg1912702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3613508, esv3613506
SamplesHG00531, HG00672
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1297e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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