A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620476



Internal ID7007347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61197633..61208600hg38UCSC Ensembl
chr9:43612172..43623150hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3810968
hg1910979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13481167, essv13481172, essv13481154, essv13481163, essv13481160, essv13481181, essv13481152, essv13481161, essv13481153, essv13481183, essv13481169, essv13481168, essv13481182, essv13481156, essv13481175, essv13481176, essv13481157, essv13481178, essv13481184, essv13481164, essv13481174, essv13481165, essv13481166, essv13481171, essv13481158, essv13481185, essv13481159, essv13481151, essv13481155, essv13481179, essv13481170, essv13481180, essv13481173, essv13481162, essv13481177
SamplesNA19141, HG01188, HG03300, HG02852, HG00879, HG02589, NA20359, HG03950, HG02621, NA19916, HG03209, NA20812, HG01757, NA19235, HG02946, HG03073, HG03058, NA20515, HG03787, HG02076, HG02108, HG02775, NA20770, HG03397, HG02884, HG03571, HG01865, HG01812, NA11881, HG01894, HG02137, HG02053, HG02763, HG01431, HG01464
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620476
Frequency
Sample Size2504
Observed Gain35
Observed Loss0
Observed Complex0
Frequencyn/a


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