A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624253



Internal ID6664420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94643661..94761810hg38UCSC Ensembl
Innerchr10:94643670..94761802hg38UCSC Ensembl
Outerchr10:94643653..94761819hg38UCSC Ensembl
chr10:96403418..96521567hg19UCSC Ensembl
Innerchr10:96403427..96521559hg19UCSC Ensembl
Outerchr10:96403410..96521576hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38118150
hg19118150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13902085
SamplesHG00185
Known GenesCYP2C18
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624253
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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