A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11661436



Internal ID4576681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158657286..158671962hg38UCSC Ensembl
chr4:159578438..159593114hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3814677
hg1914677
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602837
Supporting Variants
SamplesHG04090
Known GenesC4orf46
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11661436
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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