A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11198379



Internal ID4400093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159152363..159230598hg38UCSC Ensembl
chr3:158870152..158948387hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3878236
hg1978236
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598357
Supporting Variants
SamplesHG03919
Known GenesIQCJ, IQCJ-SCHIP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11198379
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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