A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13902091



Internal ID3903907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94724384..94768606hg38UCSC Ensembl
Innerchr10:94724384..94768606hg38UCSC Ensembl
Outerchr10:94723884..94769106hg38UCSC Ensembl
chr10:96484141..96528363hg19UCSC Ensembl
Innerchr10:96484141..96528363hg19UCSC Ensembl
Outerchr10:96483641..96528863hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3844223
hg1944223
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624256
Supporting Variants
SamplesHG00185
Known GenesCYP2C18, CYP2C19
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13902091
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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