A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11694966



Internal ID4004293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170902388..170934687hg38UCSC Ensembl
chr4:171823539..171855838hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3832300
hg1932300
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603150
Supporting Variants
SamplesHG03653
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11694966
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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