A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602460



Internal ID6989494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141203100..141215146hg38UCSC Ensembl
Innerchr4:141203107..141215139hg38UCSC Ensembl
Outerchr4:141203093..141215153hg38UCSC Ensembl
chr4:142124254..142136300hg19UCSC Ensembl
Innerchr4:142124261..142136293hg19UCSC Ensembl
Outerchr4:142124247..142136307hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3812047
hg1912047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11634974, essv11634972, essv11634970, essv11634975, essv11634976, essv11634973, essv11634971, essv11634969, essv11634977
SamplesNA19703, NA19909, HG02012, HG02442, HG02144, HG03428, HG03311, HG02429, HG02923
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602460
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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