A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616862



Internal ID7003748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34697104..34699123hg38UCSC Ensembl
Innerchr8:34697107..34699120hg38UCSC Ensembl
Outerchr8:34697101..34699126hg38UCSC Ensembl
chr8:34554622..34556641hg19UCSC Ensembl
Innerchr8:34554625..34556638hg19UCSC Ensembl
Outerchr8:34554619..34556644hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382020
hg192020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13164645
SamplesHG00421
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616862
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer