A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624362



Internal ID6664529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100454267..100509638hg38UCSC Ensembl
chr10:102214024..102269395hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3855372
hg1955372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13912977
SamplesNA06994
Known GenesSEC31B, WNT8B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624362
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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