A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893956



Internal ID19184810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:106111000..106522299hg38UCSC Ensembl
Outerchr1:106111000..106522299hg38UCSC Ensembl
Innerchr1:106653622..107064921hg19UCSC Ensembl
Outerchr1:106653622..107064921hg19UCSC Ensembl
Innerchr1:106455145..106866444hg18UCSC Ensembl
Outerchr1:106455145..106866444hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38411300
hg19411300
hg18411300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779604
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893956
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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