A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603233



Internal ID6990265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174643234..174652749hg38UCSC Ensembl
Innerchr4:174643734..174652249hg38UCSC Ensembl
Outerchr4:174642234..174653749hg38UCSC Ensembl
chr4:175564385..175573900hg19UCSC Ensembl
Innerchr4:175564885..175573400hg19UCSC Ensembl
Outerchr4:175563385..175574900hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg389516
hg199516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11711851
SamplesHG03594
Known GenesGLRA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603233
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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