A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616927



Internal ID7003813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38535795..38537560hg38UCSC Ensembl
Innerchr8:38535818..38537537hg38UCSC Ensembl
Outerchr8:38535772..38537583hg38UCSC Ensembl
chr8:38393313..38395078hg19UCSC Ensembl
Innerchr8:38393336..38395055hg19UCSC Ensembl
Outerchr8:38393290..38395101hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg381766
hg191766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13169151, essv13169149, essv13169150, essv13169148
SamplesNA18878, HG02009, HG03311, NA19472
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616927
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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