A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602861



Internal ID6989894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160105641..160159382hg38UCSC Ensembl
chr4:161026793..161080534hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3853742
hg1953742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11662792, essv11662795, essv11662802, essv11662810, essv11662800, essv11662803, essv11662794, essv11662788, essv11662798, essv11662791, essv11662799, essv11662797, essv11662805, essv11662801, essv11662807, essv11662796, essv11662804, essv11662806, essv11662789, essv11662809, essv11662808, essv11662811, essv11662793, essv11662813, essv11662814, essv11662790, essv11662812
SamplesHG01303, NA20752, NA12341, NA12812, HG00309, NA20342, HG01139, NA12878, NA20521, NA19654, HG01414, HG01707, HG01241, HG00140, HG01697, NA12043, HG02220, HG00357, HG00237, HG00288, HG00280, HG01781, HG00105, HG01509, HG00362, NA12776, NA20509
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602861
Frequency
Sample Size2504
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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