A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893075



Internal ID19183895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11989824..12147925hg38UCSC Ensembl
Outerchr18:11989824..12147925hg38UCSC Ensembl
Innerchr18:11989823..12147924hg19UCSC Ensembl
Outerchr18:11989823..12147924hg19UCSC Ensembl
Innerchr18:11979823..12137924hg18UCSC Ensembl
Outerchr18:11979823..12137924hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38158102
hg19158102
hg18158102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792596
Samples
Known GenesANKRD62, IMPA2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893075
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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