A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801371



Internal ID19181596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12265895..12276285hg38UCSC Ensembl
Innerchr10:12307894..12318284hg19UCSC Ensembl
Innerchr10:12347900..12358290hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3810391
hg1910391
hg1810391
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891756
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801371
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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