A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586921



Internal ID6974349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99389134..99400324hg38UCSC Ensembl
Innerchr1:99389134..99400324hg38UCSC Ensembl
Outerchr1:99388634..99400824hg38UCSC Ensembl
chr1:99854690..99865880hg19UCSC Ensembl
Innerchr1:99854690..99865880hg19UCSC Ensembl
Outerchr1:99854190..99866380hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3811191
hg1911191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10028028
SamplesNA18511
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586921
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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