A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1276e214



Internal ID22757170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26549527..26566959hg38UCSC Ensembl
chr7:26589146..26606578hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3817433
hg1917433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3612639, esv3612638
SamplesHG03905, NA19309, NA19439
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1276e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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