A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779604



Internal ID19159722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:106111000..106522299hg38UCSC Ensembl
Innerchr1:106653622..107064921hg19UCSC Ensembl
Innerchr1:106455145..106866444hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38411300
hg19411300
hg18411300
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893956
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=87
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779604
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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