A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599760



Internal ID6986805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16442597..16459211hg38UCSC Ensembl
Innerchr4:16442604..16459205hg38UCSC Ensembl
Outerchr4:16442591..16459218hg38UCSC Ensembl
chr4:16444220..16460834hg19UCSC Ensembl
Innerchr4:16444227..16460828hg19UCSC Ensembl
Outerchr4:16444214..16460841hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3816615
hg1916615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11360378, essv11360379, essv11360377
SamplesNA18618, NA18582, HG02070
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599760
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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