A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798140



Internal ID18828231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3611243..3618507hg38UCSC Ensembl
Innerchr18:3611241..3618506hg19UCSC Ensembl
Innerchr18:3601241..3608506hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg387265
hg197266
hg187266
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893064
Supporting Variants
Samples
Known GenesDLGAP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798140
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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