A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621478



Internal ID6661657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110984337..110998685hg38UCSC Ensembl
chr9:113746617..113760965hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3814349
hg1914349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13601054
SamplesHG02081
Known GenesLPAR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621478
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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