A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620462



Internal ID7007333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39826173..39840699hg38UCSC Ensembl
chr9:41971191..41985717hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3814527
hg1914527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1473e214
Supporting Variantsessv13472789, essv13472783, essv13472810, essv13472812, essv13472778, essv13472797, essv13472793, essv13472790, essv13472814, essv13472815, essv13472786, essv13472808, essv13472792, essv13472811, essv13472788, essv13472817, essv13472798, essv13472782, essv13472803, essv13472805, essv13472799, essv13472791, essv13472780, essv13472787, essv13472806, essv13472802, essv13472809, essv13472784, essv13472800, essv13472807, essv13472785, essv13472794, essv13472779, essv13472813, essv13472781, essv13472796, essv13472804, essv13472795, essv13472816, essv13472801
SamplesNA11829, HG03111, HG04211, NA19350, HG02382, HG00115, HG03193, NA18526, HG01051, HG03680, HG03603, NA18550, HG02151, HG03808, NA20795, HG04106, HG03746, HG03947, HG03995, NA21114, HG04029, NA19247, HG04225, HG03775, HG03781, HG03755, HG02594, HG01589, HG03720, HG03875, HG01800, NA12873, NA12046, NA21126, HG01861, HG01085, HG00310, HG00234, HG01775, HG03741
Known GenesKGFLP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620462
Frequency
Sample Size2504
Observed Gain40
Observed Loss0
Observed Complex0
Frequencyn/a


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