A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11659765



Internal ID6518884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156476571..156524165hg38UCSC Ensembl
chr4:157397723..157445317hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3847595
hg1947595
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602783
Supporting Variants
SamplesNA20541
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11659765
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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