A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801008



Internal ID19167874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:90731139..90793554hg38UCSC Ensembl
Innerchr12:91124916..91187331hg19UCSC Ensembl
Innerchr12:89649047..89711462hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3862416
hg1962416
hg1862416
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892245
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801008
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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