A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624973



Internal ID7011822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131727524..131844946hg38UCSC Ensembl
chr10:133559860..133677281hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38117423
hg19117422
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13979813, essv13979812
SamplesHG02952, NA19428
Known GenesFLJ46300
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624973
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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