A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799522



Internal ID19166167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:40657208..40685484hg38UCSC Ensembl
Innerchr18:38237172..38265448hg19UCSC Ensembl
Innerchr18:36491170..36519446hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3828277
hg1928277
hg1828277
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893094
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799522
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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