A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591125



Internal ID6631409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66638640..66649195hg38UCSC Ensembl
chr2:66865772..66876327hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3810556
hg1910556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10532382
SamplesNA18516
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591125
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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