A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv362e214



Internal ID22756256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:93158978..93201452hg38UCSC Ensembl
chr13:93811231..93853705hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3842475
hg1942475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3633191, esv3633192
SamplesHG02652, HG03963, HG04182, HG03978, HG03888, HG03814, HG01149, HG04235, HG01697, HG04200, HG03809, NA19434, NA19429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv362e214
Frequency
Sample Size2504
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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