A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555028



Internal ID18756104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9205225..9206915hg38UCSC Ensembl
Outerchr18:9205167..9206934hg38UCSC Ensembl
Innerchr18:9205223..9206913hg19UCSC Ensembl
Outerchr18:9205165..9206932hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381768
hg191768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753775
Samples
Known GenesANKRD12
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555028
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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