A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602726



Internal ID6989759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153475086..153483590hg38UCSC Ensembl
Innerchr4:153475107..153483570hg38UCSC Ensembl
Outerchr4:153475066..153483611hg38UCSC Ensembl
chr4:154396238..154404742hg19UCSC Ensembl
Innerchr4:154396259..154404722hg19UCSC Ensembl
Outerchr4:154396218..154404763hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg388505
hg198505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11655777, essv11655776, essv11655778
SamplesNA18633, HG03826, NA18559
Known GenesKIAA0922
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602726
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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