A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587862



Internal ID6975285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168370532..168374476hg38UCSC Ensembl
Innerchr1:168370532..168374476hg38UCSC Ensembl
Outerchr1:168370443..168374645hg38UCSC Ensembl
chr1:168339770..168343714hg19UCSC Ensembl
Innerchr1:168339770..168343714hg19UCSC Ensembl
Outerchr1:168339681..168343883hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg383945
hg193945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10182316
SamplesNA07357
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587862
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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