A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598305



Internal ID6985441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156741490..156743273hg38UCSC Ensembl
Innerchr3:156741507..156743256hg38UCSC Ensembl
Outerchr3:156741473..156743290hg38UCSC Ensembl
chr3:156459279..156461062hg19UCSC Ensembl
Innerchr3:156459296..156461045hg19UCSC Ensembl
Outerchr3:156459262..156461079hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg381784
hg191784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11194904
SamplesHG03780
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598305
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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