A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624960



Internal ID7011809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131446890..131640975hg38UCSC Ensembl
chr10:133245153..133473311hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38194086
hg19228159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13977653, essv13977652
SamplesHG02952, NA19428
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624960
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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