A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624313



Internal ID6664480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97431212..97441841hg38UCSC Ensembl
chr10:99190969..99201598hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3810630
hg1910630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13908165, essv13908166
SamplesNA19670, HG01551
Known GenesEXOSC1, PGAM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624313
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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