A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801501



Internal ID19168531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10181503..10200733hg38UCSC Ensembl
Innerchr18:10181500..10200730hg19UCSC Ensembl
Innerchr18:10171500..10190730hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3819231
hg1919231
hg1819231
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893072
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801501
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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