A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633191



Internal ID7020001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:93158978..93193436hg38UCSC Ensembl
chr13:93811231..93845689hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3834459
hg1934459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv362e214
Supporting Variantsessv14861097, essv14861101, essv14861107, essv14861099, essv14861098, essv14861100, essv14861106, essv14861103, essv14861104, essv14861105, essv14861102, essv14861096
SamplesHG02652, HG03963, HG04182, HG03978, HG03888, HG01149, HG04235, HG01697, HG04200, HG03809, NA19434, NA19429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633191
Frequency
Sample Size2504
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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