A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785812



Internal ID19166035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:164426611..164445504hg38UCSC Ensembl
Innerchr1:164395848..164414741hg19UCSC Ensembl
Innerchr1:162662472..162681365hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3818894
hg1918894
hg1818894
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890726
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785812
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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