A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555095



Internal ID18756171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14222599..14222746hg38UCSC Ensembl
Outerchr18:14222582..14222752hg38UCSC Ensembl
Innerchr18:14222598..14222745hg19UCSC Ensembl
Outerchr18:14222581..14222751hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753842
Samples
Known GenesANKRD20A5P
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555095
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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