A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616919



Internal ID7003805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38158909..38159796hg38UCSC Ensembl
Innerchr8:38158951..38159755hg38UCSC Ensembl
Outerchr8:38158868..38159838hg38UCSC Ensembl
chr8:38016427..38017314hg19UCSC Ensembl
Innerchr8:38016469..38017273hg19UCSC Ensembl
Outerchr8:38016386..38017356hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13169136
SamplesHG03060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616919
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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