A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893064



Internal ID18837198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3611243..3618507hg38UCSC Ensembl
Outerchr18:3611243..3618507hg38UCSC Ensembl
Innerchr18:3611241..3618506hg19UCSC Ensembl
Outerchr18:3611241..3618506hg19UCSC Ensembl
Innerchr18:3601241..3608506hg18UCSC Ensembl
Outerchr18:3601241..3608506hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg387265
hg197266
hg187266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798140
Samples
Known GenesDLGAP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893064
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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