A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1268e214



Internal ID22757162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13361855..13402951hg38UCSC Ensembl
chr7:13401480..13442576hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3841097
hg1941097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3612291, esv3612290
SamplesHG01860, HG02187
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1268e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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