A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601277



Internal ID6641534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87430386..87443786hg38UCSC Ensembl
Innerchr4:87430386..87443786hg38UCSC Ensembl
Outerchr4:87429886..87444286hg38UCSC Ensembl
chr4:88351538..88364938hg19UCSC Ensembl
Innerchr4:88351538..88364938hg19UCSC Ensembl
Outerchr4:88351038..88365438hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3813401
hg1913401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11527640, essv11527641
SamplesHG03240, HG01926
Known GenesNUDT9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601277
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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