A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11327860



Internal ID3900598
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599495
Supporting Variants
SamplesHG03557
Known GenesEVC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11327860
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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