A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1317e214



Internal ID22757211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108954936..109004438hg38UCSC Ensembl
chr7:108594993..108644495hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3849503
hg1949503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3614487, esv3614486
SamplesNA18526, NA18633, NA19086, NA18956, HG00613, HG00446
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1317e214
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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