A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622434



Internal ID7009293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14969228..15018085hg38UCSC Ensembl
chr10:15011227..15060084hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3848858
hg1948858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13704050, essv13704056, essv13704053, essv13704049, essv13704048, essv13704054, essv13704052, essv13704046, essv13704051, essv13704047, essv13704055
SamplesNA19669, NA18526, HG01277, NA19307, HG01670, HG04019, HG01049, HG02081, HG02399, NA19323, NA20528
Known GenesMEIG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622434
Frequency
Sample Size2504
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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