A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785971



Internal ID19165254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4057494..4239667hg38UCSC Ensembl
Innerchr1:4117554..4299727hg19UCSC Ensembl
Innerchr1:4017414..4199587hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38182174
hg19182174
hg18182174
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893767
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=68
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785971
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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