A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597278



Internal ID6972212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105356812..105359141hg38UCSC Ensembl
Innerchr3:105356812..105359141hg38UCSC Ensembl
Outerchr3:105356487..105359486hg38UCSC Ensembl
chr3:105075656..105077985hg19UCSC Ensembl
Innerchr3:105075656..105077985hg19UCSC Ensembl
Outerchr3:105075331..105078330hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg382330
hg192330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11093283, essv11093261, essv11093266, essv11093295, essv11093276, essv11093249, essv11093252, essv11093251, essv11093274, essv11093254, essv11093287, essv11093255, essv11093284, essv11093270, essv11093253, essv11093281, essv11093265, essv11093269, essv11093301, essv11093267, essv11093294, essv11093285, essv11093297, essv11093250, essv11093268, essv11093258, essv11093292, essv11093259, essv11093286, essv11093271, essv11093247, essv11093303, essv11093282, essv11093256, essv11093299, essv11093293, essv11093244, essv11093291, essv11093260, essv11093288, essv11093279, essv11093248, essv11093300, essv11093302, essv11093277, essv11093278, essv11093272, essv11093245, essv11093304, essv11093280, essv11093263, essv11093296, essv11093257, essv11093246, essv11093290, essv11093262, essv11093273, essv11093264, essv11093298, essv11093243, essv11093289, essv11093275
SamplesNA20762, NA20588, HG01746, HG01098, NA20891, HG01624, NA12814, HG00315, HG00151, NA20512, HG00640, HG00364, HG02215, NA20517, HG01461, HG00327, HG01488, HG00129, HG03234, HG00158, HG02143, HG00120, HG00335, HG03777, HG01259, NA12760, NA20524, HG01790, NA20521, NA20810, HG00132, HG01077, HG04180, NA20770, HG01094, NA19084, HG00350, NA20581, HG01593, HG01680, HG00240, HG01589, HG03743, HG00336, HG00285, NA12873, NA06986, HG01991, HG01491, HG02238, HG01935, NA20849, HG00342, HG00288, HG01254, NA12830, HG01089, HG03916, HG00280, HG03922, HG00345, HG01776
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597278
Frequency
Sample Size2504
Observed Gain0
Observed Loss62
Observed Complex0
Frequencyn/a


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