A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624259



Internal ID6664426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94737559..94799350hg38UCSC Ensembl
Innerchr10:94737561..94799348hg38UCSC Ensembl
Outerchr10:94737557..94799352hg38UCSC Ensembl
chr10:96497316..96559107hg19UCSC Ensembl
Innerchr10:96497318..96559105hg19UCSC Ensembl
Outerchr10:96497314..96559109hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3861792
hg1961792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv160e214
Supporting Variantsessv13902095
SamplesHG00268
Known GenesCYP2C19
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624259
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