A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3592935



Internal ID6633218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:152505792..152527937hg38UCSC Ensembl
chr2:153362306..153384451hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3822146
hg1922146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10713112, essv10713113
SamplesHG03160, NA19355
Known GenesFMNL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3592935
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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