A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599741



Internal ID6640004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15701308..15709562hg38UCSC Ensembl
chr4:15702931..15711185hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg388255
hg198255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11360146, essv11360156, essv11360145, essv11360149, essv11360154, essv11360150, essv11360163, essv11360157, essv11360142, essv11360143, essv11360166, essv11360164, essv11360144, essv11360151, essv11360158, essv11360153, essv11360148, essv11360152, essv11360165, essv11360162, essv11360161, essv11360155, essv11360160, essv11360159, essv11360147
SamplesHG03717, HG03963, HG03018, HG03808, HG04185, NA20884, HG04029, HG03784, HG03862, HG03844, HG03718, HG03491, HG03775, HG04180, HG03021, HG03742, NA20867, NA20881, HG03991, HG04025, HG02685, HG04080, HG04209, HG03684, HG03985
Known GenesBST1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599741
Frequency
Sample Size2504
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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