A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13902095



Internal ID3903911
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624259
Supporting Variants
SamplesHG00268
Known GenesCYP2C19
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13902095
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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