A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599495



Internal ID6986541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5761228..5780036hg38UCSC Ensembl
chr4:5762955..5781763hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3818809
hg1918809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11327860, essv11327858, essv11327861, essv11327859
SamplesHG03372, HG03485, NA18871, HG03557
Known GenesEVC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599495
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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