A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1312e214



Internal ID22757206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95702481..95748496hg38UCSC Ensembl
chr7:95331793..95377808hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3846016
hg1946016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3614199, esv3614198
SamplesHG01860, HG02142, HG00956, NA18608, HG02179, HG01862, HG02353
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1312e214
Frequency
Sample Size2504
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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