A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10160880



Internal ID162696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158757128..158758220hg38UCSC Ensembl
Innerchr1:158757128..158758220hg38UCSC Ensembl
Outerchr1:158756699..158758639hg38UCSC Ensembl
chr1:158726918..158728010hg19UCSC Ensembl
Innerchr1:158726918..158728010hg19UCSC Ensembl
Outerchr1:158726489..158728429hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381093
hg191093
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3587682
Supporting Variants
SamplesNA21143
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10160880
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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