A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587874



Internal ID6975297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168886563..168887481hg38UCSC Ensembl
Innerchr1:168886565..168887479hg38UCSC Ensembl
Outerchr1:168886561..168887483hg38UCSC Ensembl
chr1:168855801..168856719hg19UCSC Ensembl
Innerchr1:168855803..168856717hg19UCSC Ensembl
Outerchr1:168855799..168856721hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10183244
SamplesNA18988
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587874
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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